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- [1] Analysis of the ABCA4 c.[2588G>C;5603A>T] Allele in the Australian PopulationRETINAL DEGENERATIVE DISEASES: MECHANISMS AND EXPERIMENTAL THERAPY, 2019, 1185 : 269 - 273Thompson, Jennifer A.论文数: 0 引用数: 0 h-index: 0机构: Sir Charles Gairdner Hosp, Dept Med Technol & Phys, Australian Inherited Retinal Dis Registry & DNA B, Perth, WA, Australia Sir Charles Gairdner Hosp, Dept Med Technol & Phys, Australian Inherited Retinal Dis Registry & DNA B, Perth, WA, AustraliaChiang, John论文数: 0 引用数: 0 h-index: 0机构: Mol Vis Lab, Hillsboro, OR USA Sir Charles Gairdner Hosp, Dept Med Technol & Phys, Australian Inherited Retinal Dis Registry & DNA B, Perth, WA, AustraliaDe Roach, John N.论文数: 0 引用数: 0 h-index: 0机构: Sir Charles Gairdner Hosp, Dept Med Technol & Phys, Australian Inherited Retinal Dis Registry & DNA B, Perth, WA, Australia Univ Western Australia, Ctr Ophthalmol & Visual Sci, Crawley, WA, Australia Sir Charles Gairdner Hosp, Dept Med Technol & Phys, Australian Inherited Retinal Dis Registry & DNA B, Perth, WA, AustraliaMcLaren, Terri L.论文数: 0 引用数: 0 h-index: 0机构: Sir Charles Gairdner Hosp, Dept Med Technol & Phys, Australian Inherited Retinal Dis Registry & DNA B, Perth, WA, Australia Univ Western Australia, Ctr Ophthalmol & Visual Sci, Crawley, WA, Australia Sir Charles Gairdner Hosp, Dept Med Technol & Phys, Australian Inherited Retinal Dis Registry & DNA B, Perth, WA, AustraliaChen, Fred K.论文数: 0 引用数: 0 h-index: 0机构: Sir Charles Gairdner Hosp, Dept Med Technol & Phys, Australian Inherited Retinal Dis Registry & DNA B, Perth, WA, Australia Univ Western Australia, Ctr Ophthalmol & Visual Sci, Crawley, WA, Australia Lions Eye Inst, Ocular Tissue Engn Lab, Perth, WA, Australia Royal Perth Hosp, Dept Ophthalmol, Perth, WA, Australia Sir Charles Gairdner Hosp, Dept Med Technol & Phys, Australian Inherited Retinal Dis Registry & DNA B, Perth, WA, AustraliaHoffmann, Ling论文数: 0 引用数: 0 h-index: 0机构: Sir Charles Gairdner Hosp, Dept Med Technol & Phys, Australian Inherited Retinal Dis Registry & DNA B, Perth, WA, Australia Sir Charles Gairdner Hosp, Dept Med Technol & Phys, Australian Inherited Retinal Dis Registry & DNA B, Perth, WA, AustraliaCampbell, Isabella论文数: 0 引用数: 0 h-index: 0机构: Sir Charles Gairdner Hosp, Dept Med Technol & Phys, Australian Inherited Retinal Dis Registry & DNA B, Perth, WA, Australia Sir Charles Gairdner Hosp, Dept Med Technol & Phys, Australian Inherited Retinal Dis Registry & DNA B, Perth, WA, AustraliaLamey, Tina M.论文数: 0 引用数: 0 h-index: 0机构: Sir Charles Gairdner Hosp, Dept Med Technol & Phys, Australian Inherited Retinal Dis Registry & DNA B, Perth, WA, Australia Univ Western Australia, Ctr Ophthalmol & Visual Sci, Crawley, WA, Australia Sir Charles Gairdner Hosp, Dept Med Technol & Phys, Australian Inherited Retinal Dis Registry & DNA B, Perth, WA, Australia
- [2] Generation of two induced pluripotent stem cell lines from a patient with Stargardt Macular Dystrophy caused by the c.768G > T and c.6079C > T mutations in ABCA4STEM CELL RESEARCH, 2020, 48Jennings, Luke论文数: 0 引用数: 0 h-index: 0机构: Univ Western Australia, Ctr Ophthalmol & Visual Sci, Perth, WA, Australia Lions Eye Inst, Nedlands, WA, Australia Univ Western Australia, Ctr Ophthalmol & Visual Sci, Perth, WA, AustraliaZhang, Dan论文数: 0 引用数: 0 h-index: 0机构: Lions Eye Inst, Nedlands, WA, Australia Univ Western Australia, Ctr Ophthalmol & Visual Sci, Perth, WA, AustraliaChen, Shang-Chih论文数: 0 引用数: 0 h-index: 0机构: Lions Eye Inst, Nedlands, WA, Australia Univ Western Australia, Ctr Ophthalmol & Visual Sci, Perth, WA, AustraliaMoon, Sang Yoon论文数: 0 引用数: 0 h-index: 0机构: Univ Western Australia, Ctr Ophthalmol & Visual Sci, Perth, WA, Australia Univ Western Australia, Ctr Ophthalmol & Visual Sci, Perth, WA, AustraliaLamey, Tina论文数: 0 引用数: 0 h-index: 0机构: Univ Western Australia, Ctr Ophthalmol & Visual Sci, Perth, WA, Australia Sir Charles Gairdner Hosp, Dept Med Technol & Phys, Australian Inherited Retinal Dis Registry & DNA B, Perth, WA, Australia Univ Western Australia, Ctr Ophthalmol & Visual Sci, Perth, WA, AustraliaThompson, Jennifer A.论文数: 0 引用数: 0 h-index: 0机构: Sir Charles Gairdner Hosp, Dept Med Technol & Phys, Australian Inherited Retinal Dis Registry & DNA B, Perth, WA, Australia Univ Western Australia, Ctr Ophthalmol & Visual Sci, Perth, WA, AustraliaMcLaren, Terri论文数: 0 引用数: 0 h-index: 0机构: Univ Western Australia, Ctr Ophthalmol & Visual Sci, Perth, WA, Australia Sir Charles Gairdner Hosp, Dept Med Technol & Phys, Australian Inherited Retinal Dis Registry & DNA B, Perth, WA, Australia Univ Western Australia, Ctr Ophthalmol & Visual Sci, Perth, WA, AustraliaDe Roach, John N.论文数: 0 引用数: 0 h-index: 0机构: Univ Western Australia, Ctr Ophthalmol & Visual Sci, Perth, WA, Australia Sir Charles Gairdner Hosp, Dept Med Technol & Phys, Australian Inherited Retinal Dis Registry & DNA B, Perth, WA, Australia Univ Western Australia, Ctr Ophthalmol & Visual Sci, Perth, WA, AustraliaChen, Fred K.论文数: 0 引用数: 0 h-index: 0机构: Univ Western Australia, Ctr Ophthalmol & Visual Sci, Perth, WA, Australia Lions Eye Inst, Nedlands, WA, Australia Sir Charles Gairdner Hosp, Dept Med Technol & Phys, Australian Inherited Retinal Dis Registry & DNA B, Perth, WA, Australia Royal Perth Hosp, Dept Ophthalmol, Perth, WA, Australia Univ Western Australia, Ctr Ophthalmol & Visual Sci, Perth, WA, AustraliaMcLenachan, Samuel论文数: 0 引用数: 0 h-index: 0机构: Univ Western Australia, Ctr Ophthalmol & Visual Sci, Perth, WA, Australia Lions Eye Inst, Nedlands, WA, Australia Univ Western Australia, Ctr Ophthalmol & Visual Sci, Perth, WA, Australia
- [3] Oligonucleotide-based splice correction of the ABCA4 c.5461-10T>C mutation in Stargardt disease type 1INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2018, 59 (09)Dulla, Kalyan论文数: 0 引用数: 0 h-index: 0机构: ProQR Therapeut, Leiden, Netherlands ProQR Therapeut, Leiden, NetherlandsYilmaz-Elis, Seda论文数: 0 引用数: 0 h-index: 0机构: ProQR Therapeut, Leiden, Netherlands ProQR Therapeut, Leiden, NetherlandsMiao, Jiayi论文数: 0 引用数: 0 h-index: 0机构: ProQR Therapeut, Leiden, Netherlands ProQR Therapeut, Leiden, NetherlandsSchmidt, Iris论文数: 0 引用数: 0 h-index: 0机构: ProQR Therapeut, Leiden, Netherlands ProQR Therapeut, Leiden, NetherlandsSchulkens, Iris论文数: 0 引用数: 0 h-index: 0机构: ProQR Therapeut, Leiden, Netherlands ProQR Therapeut, Leiden, NetherlandsChan, Hee Lam论文数: 0 引用数: 0 h-index: 0机构: ProQR Therapeut, Leiden, Netherlands ProQR Therapeut, Leiden, NetherlandsAdamson, Peter S.论文数: 0 引用数: 0 h-index: 0机构: ProQR Therapeut, Leiden, Netherlands ProQR Therapeut, Leiden, Netherlands
- [4] Generation of three induced pluripotent stem cell lines from a patient with Usher syndrome caused by biallelic c.949C > A and c.1256G > T mutations in the USH2A geneSTEM CELL RESEARCH, 2021, 50Zaw, Khine论文数: 0 引用数: 0 h-index: 0机构: Lions Eye Inst, Ocular Tissue Engn Lab, Nedlands, WA, Australia Murdoch Univ, Ctr Mol Med & Innovat Therapeut, Murdoch, WA, Australia Mahidol Univ, Fac Med, Dept Biochem, Siriraj Hosp, Bangkok, Thailand Lions Eye Inst, Ocular Tissue Engn Lab, Nedlands, WA, AustraliaWong, Elaine Y. M.论文数: 0 引用数: 0 h-index: 0机构: Ear Sci Inst Australia, Nedlands, WA, Australia Curtin Univ, Fac Hlth Sci, Sch Pharm & Biomed Sci, Bentley, WA, Australia Univ Western Australia, Ear Sci Ctr, Nedlands, WA, Australia Lions Eye Inst, Ocular Tissue Engn Lab, Nedlands, WA, AustraliaZhang, Xiao论文数: 0 引用数: 0 h-index: 0机构: Lions Eye Inst, Ocular Tissue Engn Lab, Nedlands, WA, Australia Univ Western Australia, Ctr Ophthalmol & Visual Sci, Nedlands, WA, Australia Lions Eye Inst, Ocular Tissue Engn Lab, Nedlands, WA, AustraliaZhang, Dan论文数: 0 引用数: 0 h-index: 0机构: Lions Eye Inst, Ocular Tissue Engn Lab, Nedlands, WA, Australia Lions Eye Inst, Ocular Tissue Engn Lab, Nedlands, WA, AustraliaChen, Shang-Chih论文数: 0 引用数: 0 h-index: 0机构: Lions Eye Inst, Ocular Tissue Engn Lab, Nedlands, WA, Australia Lions Eye Inst, Ocular Tissue Engn Lab, Nedlands, WA, AustraliaThompson, Jennifer A.论文数: 0 引用数: 0 h-index: 0机构: Sir Charles Gairdner Hosp, Dept Med Technol & Phys, Australian Inherited Retinal Dis Registry & DNA B, Perth, WA, Australia Lions Eye Inst, Ocular Tissue Engn Lab, Nedlands, WA, AustraliaLamey, Tina论文数: 0 引用数: 0 h-index: 0机构: Univ Western Australia, Ctr Ophthalmol & Visual Sci, Nedlands, WA, Australia Sir Charles Gairdner Hosp, Dept Med Technol & Phys, Australian Inherited Retinal Dis Registry & DNA B, Perth, WA, Australia Lions Eye Inst, Ocular Tissue Engn Lab, Nedlands, WA, AustraliaMcLaren, Terri论文数: 0 引用数: 0 h-index: 0机构: Univ Western Australia, Ctr Ophthalmol & Visual Sci, Nedlands, WA, Australia Sir Charles Gairdner Hosp, Dept Med Technol & Phys, Australian Inherited Retinal Dis Registry & DNA B, Perth, WA, Australia Lions Eye Inst, Ocular Tissue Engn Lab, Nedlands, WA, AustraliaDe Roach, John N.论文数: 0 引用数: 0 h-index: 0机构: Univ Western Australia, Ctr Ophthalmol & Visual Sci, Nedlands, WA, Australia Sir Charles Gairdner Hosp, Dept Med Technol & Phys, Australian Inherited Retinal Dis Registry & DNA B, Perth, WA, Australia Lions Eye Inst, Ocular Tissue Engn Lab, Nedlands, WA, AustraliaWilton, Steve D.论文数: 0 引用数: 0 h-index: 0机构: Murdoch Univ, Ctr Mol Med & Innovat Therapeut, Murdoch, WA, Australia Univ Western Australia, Perron Inst Neurol & Translat Sci, Perth, WA, Australia Univ Western Australia, Ctr Neuromuscular & Neurol Disorders, Perth, WA, Australia Lions Eye Inst, Ocular Tissue Engn Lab, Nedlands, WA, AustraliaFletcher, Sue论文数: 0 引用数: 0 h-index: 0机构: Murdoch Univ, Ctr Mol Med & Innovat Therapeut, Murdoch, WA, Australia Univ Western Australia, Perron Inst Neurol & Translat Sci, Perth, WA, Australia Univ Western Australia, Ctr Neuromuscular & Neurol Disorders, Perth, WA, Australia Lions Eye Inst, Ocular Tissue Engn Lab, Nedlands, WA, Australia论文数: 引用数: h-index:机构:Atlas, Marcus D.论文数: 0 引用数: 0 h-index: 0机构: Ear Sci Inst Australia, Nedlands, WA, Australia Univ Western Australia, Ear Sci Ctr, Nedlands, WA, Australia Lions Eye Inst, Ocular Tissue Engn Lab, Nedlands, WA, AustraliaChen, Fred K.论文数: 0 引用数: 0 h-index: 0机构: Lions Eye Inst, Ocular Tissue Engn Lab, Nedlands, WA, Australia Univ Western Australia, Ctr Ophthalmol & Visual Sci, Nedlands, WA, Australia Sir Charles Gairdner Hosp, Dept Med Technol & Phys, Australian Inherited Retinal Dis Registry & DNA B, Perth, WA, Australia Royal Perth Hosp, Dept Ophthalmol, Perth, WA, Australia Perth Childrens Hosp, Dept Ophthalmol, Nedlands, WA, Australia Lions Eye Inst, Ocular Tissue Engn Lab, Nedlands, WA, AustraliaMcLenachan, Samuel论文数: 0 引用数: 0 h-index: 0机构: Lions Eye Inst, Ocular Tissue Engn Lab, Nedlands, WA, Australia Univ Western Australia, Ctr Ophthalmol & Visual Sci, Nedlands, WA, Australia Lions Eye Inst, Ocular Tissue Engn Lab, Nedlands, WA, Australia
- [5] The intronic ABCA4 c.5461-10T>C variant, frequently seen in patients with Stargardt disease, causes splice defects and reduced ABCA4 protein levelACTA OPHTHALMOLOGICA, 2017, 95 (03) : 240 - 246Aukrust, Ingvild论文数: 0 引用数: 0 h-index: 0机构: Haukeland Hosp, Ctr Med Genet & Mol Med, Jonas Lies Vei 87, N-5021 Bergen, Norway Haukeland Hosp, Ctr Med Genet & Mol Med, Jonas Lies Vei 87, N-5021 Bergen, NorwayJansson, Ragnhild W.论文数: 0 引用数: 0 h-index: 0机构: Haukeland Hosp, Dept Ophthalmol, Bergen, Norway Univ Bergen, Dept Clin Med, Bergen, Norway Haukeland Hosp, Ctr Med Genet & Mol Med, Jonas Lies Vei 87, N-5021 Bergen, NorwayBredrup, Cecilie论文数: 0 引用数: 0 h-index: 0机构: Haukeland Hosp, Dept Ophthalmol, Bergen, Norway Haukeland Hosp, Ctr Med Genet & Mol Med, Jonas Lies Vei 87, N-5021 Bergen, NorwayRusaas, Hilde E.论文数: 0 引用数: 0 h-index: 0机构: Haukeland Hosp, Ctr Med Genet & Mol Med, Jonas Lies Vei 87, N-5021 Bergen, Norway Haukeland Hosp, Ctr Med Genet & Mol Med, Jonas Lies Vei 87, N-5021 Bergen, NorwayBerland, Siren论文数: 0 引用数: 0 h-index: 0机构: Haukeland Hosp, Ctr Med Genet & Mol Med, Jonas Lies Vei 87, N-5021 Bergen, Norway Haukeland Hosp, Ctr Med Genet & Mol Med, Jonas Lies Vei 87, N-5021 Bergen, NorwayJorgensen, Agnete论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp North Norway, Div Child & Adolescent Hlth, Med Genet Dept, Tromso, Norway Haukeland Hosp, Ctr Med Genet & Mol Med, Jonas Lies Vei 87, N-5021 Bergen, NorwayHaug, Marte G.论文数: 0 引用数: 0 h-index: 0机构: St Olavs Univ Hosp, Dept Pathol & Med Genet, Trondheim, Norway Haukeland Hosp, Ctr Med Genet & Mol Med, Jonas Lies Vei 87, N-5021 Bergen, NorwayRodahl, Eyvind论文数: 0 引用数: 0 h-index: 0机构: Haukeland Hosp, Dept Ophthalmol, Bergen, Norway Univ Bergen, Dept Clin Med, Bergen, Norway Haukeland Hosp, Ctr Med Genet & Mol Med, Jonas Lies Vei 87, N-5021 Bergen, NorwayHouge, Gunnar论文数: 0 引用数: 0 h-index: 0机构: Haukeland Hosp, Ctr Med Genet & Mol Med, Jonas Lies Vei 87, N-5021 Bergen, Norway Haukeland Hosp, Ctr Med Genet & Mol Med, Jonas Lies Vei 87, N-5021 Bergen, NorwayKnappskog, Per M.论文数: 0 引用数: 0 h-index: 0机构: Haukeland Hosp, Ctr Med Genet & Mol Med, Jonas Lies Vei 87, N-5021 Bergen, Norway Univ Bergen, Dept Clin Sci, Bergen, Norway Haukeland Hosp, Ctr Med Genet & Mol Med, Jonas Lies Vei 87, N-5021 Bergen, Norway
- [6] The impact of the c.5603A>T hypomorphic variant on founder mutation screening of ABCA4 for Stargardt disease in South AfricaMOLECULAR VISION, 2020, 26 : 613 - 622Midgley, Nicole论文数: 0 引用数: 0 h-index: 0机构: Univ Cape Town, UCT MRC Genom & Precis Med Res Unit, Div Human Genet, Dept Pathol,Inst Infect Dis & Mol Med, Cape Town, South Africa Univ Cape Town, UCT MRC Genom & Precis Med Res Unit, Div Human Genet, Dept Pathol,Inst Infect Dis & Mol Med, Cape Town, South AfricaRoberts, Lisa论文数: 0 引用数: 0 h-index: 0机构: Univ Cape Town, UCT MRC Genom & Precis Med Res Unit, Div Human Genet, Dept Pathol,Inst Infect Dis & Mol Med, Cape Town, South Africa Univ Cape Town, UCT MRC Genom & Precis Med Res Unit, Div Human Genet, Dept Pathol,Inst Infect Dis & Mol Med, Cape Town, South AfricaRebello, George论文数: 0 引用数: 0 h-index: 0机构: Univ Cape Town, UCT MRC Genom & Precis Med Res Unit, Div Human Genet, Dept Pathol,Inst Infect Dis & Mol Med, Cape Town, South Africa Univ Cape Town, UCT MRC Genom & Precis Med Res Unit, Div Human Genet, Dept Pathol,Inst Infect Dis & Mol Med, Cape Town, South AfricaRamesar, Raj论文数: 0 引用数: 0 h-index: 0机构: Univ Cape Town, UCT MRC Genom & Precis Med Res Unit, Div Human Genet, Dept Pathol,Inst Infect Dis & Mol Med, Cape Town, South Africa Univ Cape Town, UCT MRC Genom & Precis Med Res Unit, Div Human Genet, Dept Pathol,Inst Infect Dis & Mol Med, Cape Town, South Africa
- [7] Induced pluripotent stem cell line BIOi003-A from a patient with ABCA4-associated retinal dystrophy carrying compound heterozygous c. (1222C>T;2919-884G>T) variants in ABCA4STEM CELL RESEARCH, 2022, 64Tian, Lu论文数: 0 引用数: 0 h-index: 0机构: Capital Med Univ, Beijing Tongren Hosp, Beijing Inst Ophthalmol, Beijing Tongren Eye Ctr,Beijing Ophthalmol & Visua, Beijing, Peoples R China Capital Med Univ, Beijing Tongren Hosp, Beijing Inst Ophthalmol, Beijing Tongren Eye Ctr,Beijing Ophthalmol & Visua, Beijing, Peoples R ChinaZhang, Xiao-hui论文数: 0 引用数: 0 h-index: 0机构: Capital Med Univ, Beijing Tongren Hosp, Beijing Inst Ophthalmol, Beijing Tongren Eye Ctr,Beijing Ophthalmol & Visua, Beijing, Peoples R China Capital Med Univ, Beijing Tongren Hosp, Beijing Inst Ophthalmol, Beijing Tongren Eye Ctr,Beijing Ophthalmol & Visua, Beijing, Peoples R ChinaXu, Ke论文数: 0 引用数: 0 h-index: 0机构: Capital Med Univ, Beijing Tongren Hosp, Beijing Inst Ophthalmol, Beijing Tongren Eye Ctr,Beijing Ophthalmol & Visua, Beijing, Peoples R China Capital Med Univ, Beijing Tongren Hosp, Beijing Inst Ophthalmol, Beijing Tongren Eye Ctr,Beijing Ophthalmol & Visua, Beijing, Peoples R ChinaLi, Yang论文数: 0 引用数: 0 h-index: 0机构: Capital Med Univ, Beijing Tongren Hosp, Beijing Inst Ophthalmol, Beijing Tongren Eye Ctr,Beijing Ophthalmol & Visua, Beijing, Peoples R China Capital Med Univ, Beijing Tongren Hosp, Beijing Inst Ophthalmol, Beijing Tongren Eye Ctr,Beijing Ophthalmol & Visua, Beijing, Peoples R China
- [8] Using induced pluripotent stem cell-derived retinal pigment epithelial cells to model splicing defects of ABCA4 c.5461-10T>C detected in an Australian Stargardt disease cohortINVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2021, 62 (08)Huang, Di论文数: 0 引用数: 0 h-index: 0机构: Murdoch Univ, Ctr Mol Med & Innovat Therapeut, Perth, WA, Australia Perron Inst Neurol & Translat Sci, Ctr Neuromuscular & Neurol Disorders, Perth, WA, Australia Murdoch Univ, Ctr Mol Med & Innovat Therapeut, Perth, WA, AustraliaThompson, Jennifer A.论文数: 0 引用数: 0 h-index: 0机构: Sir Charles Gairdner Hosp, Australian Inherited Retinal Dis Registry, Dept Med Technol & Phys, Nedlands, WA, Australia Sir Charles Gairdner Hosp, DNA Bank, Dept Med Technol & Phys, Nedlands, WA, Australia Murdoch Univ, Ctr Mol Med & Innovat Therapeut, Perth, WA, AustraliaMcLenachan, Samuel论文数: 0 引用数: 0 h-index: 0机构: Univ Western Australia, Ctr Ophthalmol & Visual Sci, Perth, WA, Australia Murdoch Univ, Ctr Mol Med & Innovat Therapeut, Perth, WA, AustraliaChen, Shang-Chih论文数: 0 引用数: 0 h-index: 0机构: Univ Western Australia, Ctr Ophthalmol & Visual Sci, Perth, WA, Australia Lions Eye Inst, Nedlands, WA, Australia Murdoch Univ, Ctr Mol Med & Innovat Therapeut, Perth, WA, AustraliaZhang, Dan论文数: 0 引用数: 0 h-index: 0机构: Univ Western Australia, Ctr Ophthalmol & Visual Sci, Perth, WA, Australia Lions Eye Inst, Nedlands, WA, Australia Murdoch Univ, Ctr Mol Med & Innovat Therapeut, Perth, WA, AustraliaJeffery, Rachael C. Heath论文数: 0 引用数: 0 h-index: 0机构: Univ Western Australia, Ctr Ophthalmol & Visual Sci, Perth, WA, Australia Lions Eye Inst, Nedlands, WA, Australia Murdoch Univ, Ctr Mol Med & Innovat Therapeut, Perth, WA, AustraliaAttia, Mary论文数: 0 引用数: 0 h-index: 0机构: Univ Western Australia, Ctr Ophthalmol & Visual Sci, Perth, WA, Australia Lions Eye Inst, Nedlands, WA, Australia Murdoch Univ, Ctr Mol Med & Innovat Therapeut, Perth, WA, AustraliaMcLaren, Terri L.论文数: 0 引用数: 0 h-index: 0机构: Sir Charles Gairdner Hosp, Australian Inherited Retinal Dis Registry, Dept Med Technol & Phys, Nedlands, WA, Australia Sir Charles Gairdner Hosp, DNA Bank, Dept Med Technol & Phys, Nedlands, WA, Australia Univ Western Australia, Ctr Ophthalmol & Visual Sci, Perth, WA, Australia Murdoch Univ, Ctr Mol Med & Innovat Therapeut, Perth, WA, AustraliaLamey, Tina M.论文数: 0 引用数: 0 h-index: 0机构: Sir Charles Gairdner Hosp, Australian Inherited Retinal Dis Registry, Dept Med Technol & Phys, Nedlands, WA, Australia Sir Charles Gairdner Hosp, DNA Bank, Dept Med Technol & Phys, Nedlands, WA, Australia Univ Western Australia, Ctr Ophthalmol & Visual Sci, Perth, WA, Australia Murdoch Univ, Ctr Mol Med & Innovat Therapeut, Perth, WA, AustraliaDe Roach, John N.论文数: 0 引用数: 0 h-index: 0机构: Sir Charles Gairdner Hosp, Australian Inherited Retinal Dis Registry, Dept Med Technol & Phys, Nedlands, WA, Australia Sir Charles Gairdner Hosp, DNA Bank, Dept Med Technol & Phys, Nedlands, WA, Australia Univ Western Australia, Ctr Ophthalmol & Visual Sci, Perth, WA, Australia Murdoch Univ, Ctr Mol Med & Innovat Therapeut, Perth, WA, AustraliaAung-Htut, May Thandar论文数: 0 引用数: 0 h-index: 0机构: Murdoch Univ, Ctr Mol Med & Innovat Therapeut, Perth, WA, Australia Perron Inst Neurol & Translat Sci, Ctr Neuromuscular & Neurol Disorders, Perth, WA, Australia Murdoch Univ, Ctr Mol Med & Innovat Therapeut, Perth, WA, AustraliaAdams, Abbie论文数: 0 引用数: 0 h-index: 0机构: Murdoch Univ, Ctr Mol Med & Innovat Therapeut, Perth, WA, Australia Murdoch Univ, Ctr Mol Med & Innovat Therapeut, Perth, WA, AustraliaFletcher, Sue论文数: 0 引用数: 0 h-index: 0机构: Murdoch Univ, Ctr Mol Med & Innovat Therapeut, Perth, WA, Australia Perron Inst Neurol & Translat Sci, Ctr Neuromuscular & Neurol Disorders, Perth, WA, Australia Murdoch Univ, Ctr Mol Med & Innovat Therapeut, Perth, WA, AustraliaWilton, Steve论文数: 0 引用数: 0 h-index: 0机构: Murdoch Univ, Ctr Mol Med & Innovat Therapeut, Perth, WA, Australia Perron Inst Neurol & Translat Sci, Ctr Neuromuscular & Neurol Disorders, Perth, WA, Australia Murdoch Univ, Ctr Mol Med & Innovat Therapeut, Perth, WA, AustraliaChen, Fred Kuanfu论文数: 0 引用数: 0 h-index: 0机构: Univ Western Australia, Ctr Ophthalmol & Visual Sci, Perth, WA, Australia Lions Eye Inst, Nedlands, WA, Australia Murdoch Univ, Ctr Mol Med & Innovat Therapeut, Perth, WA, Australia
- [9] QR-1011 corrects splicing in the Stargardt disease type 1-causing variant ABCA4 c.5461-10T>CINVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2022, 63 (07)Kaltak, Melita论文数: 0 引用数: 0 h-index: 0机构: ProQR Therapeut NV, Leiden, Zuid Holland, Netherlands Radboud Univ Nijmegen, Nijmegen, Gelderland, Netherlands ProQR Therapeut NV, Leiden, Zuid Holland, Netherlandsde Bruijn, Petra论文数: 0 引用数: 0 h-index: 0机构: ProQR Therapeut NV, Leiden, Zuid Holland, Netherlands ProQR Therapeut NV, Leiden, Zuid Holland, NetherlandsLee, Sang-Eun论文数: 0 引用数: 0 h-index: 0机构: UCL, Inst Ophthalmol, London, England ProQR Therapeut NV, Leiden, Zuid Holland, NetherlandsPiccolo, Davide论文数: 0 引用数: 0 h-index: 0机构: UCL, Inst Ophthalmol, London, England ProQR Therapeut NV, Leiden, Zuid Holland, NetherlandsDulla, Kalyan论文数: 0 引用数: 0 h-index: 0机构: ProQR Therapeut NV, Leiden, Zuid Holland, Netherlands ProQR Therapeut NV, Leiden, Zuid Holland, NetherlandsCollin, Rob W. J.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Nijmegen, Gelderland, Netherlands ProQR Therapeut NV, Leiden, Zuid Holland, NetherlandsCheetham, Michael E.论文数: 0 引用数: 0 h-index: 0机构: UCL, Inst Ophthalmol, London, England ProQR Therapeut NV, Leiden, Zuid Holland, NetherlandsPlatenburg, Gerard论文数: 0 引用数: 0 h-index: 0机构: ProQR Therapeut NV, Leiden, Zuid Holland, Netherlands ProQR Therapeut NV, Leiden, Zuid Holland, NetherlandsSwildens, Jim论文数: 0 引用数: 0 h-index: 0机构: ProQR Therapeut NV, Leiden, Zuid Holland, Netherlands ProQR Therapeut NV, Leiden, Zuid Holland, Netherlands
- [10] Correction of the Splicing Defect Caused by a Recurrent Variant in ABCA4 (c.769-784C>T) That Underlies Stargardt DiseaseCELLS, 2022, 11 (24)Tomkiewicz, Tomasz Z. Z.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6525 GA Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Donders Inst Brain Cognit & Behaviou r, NL-6525 GA Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6525 GA Nijmegen, NetherlandsNieuwenhuis, Sara E. E.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6525 GA Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Donders Inst Brain Cognit & Behaviou r, NL-6525 GA Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6525 GA Nijmegen, NetherlandsCremers, Frans P. M.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6525 GA Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Donders Inst Brain Cognit & Behaviou r, NL-6525 GA Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6525 GA Nijmegen, NetherlandsGaranto, Alejandro论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Amalia Childrens Hosp, Dept Pediat,Human Genet & Radboud Inst Mol Life Sc, NL-6525 GA Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6525 GA Nijmegen, NetherlandsCollin, Rob W. J.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6525 GA Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Donders Inst Brain Cognit & Behaviou r, NL-6525 GA Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6525 GA Nijmegen, Netherlands