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- [1] A novel ELP1 mutation impairs the function of the Elongator complex and causes a severe neurodevelopmental phenotypeJOURNAL OF HUMAN GENETICS, 2023, 68 (07) : 445 - 453Kojic, Marija论文数: 0 引用数: 0 h-index: 0机构: Univ Queensland, Frazer Inst, Woolloongabba, Qld 4102, Australia Univ Queensland, Frazer Inst, Woolloongabba, Qld 4102, AustraliaAbbassi, Nour E. H.论文数: 0 引用数: 0 h-index: 0机构: Jagiellonian Univ, Malopolska Ctr Biotechnol, Krakow, Poland Med Univ Warsaw, Postgrad Sch Mol Med, PL-02091 Warsaw, Poland Univ Queensland, Frazer Inst, Woolloongabba, Qld 4102, AustraliaLin, Ting-Yu论文数: 0 引用数: 0 h-index: 0机构: Jagiellonian Univ, Malopolska Ctr Biotechnol, Krakow, Poland Univ Queensland, Frazer Inst, Woolloongabba, Qld 4102, Australia论文数: 引用数: h-index:机构:Wakeling, Emma L.论文数: 0 引用数: 0 h-index: 0机构: Great Ormond St Hosp Children NHS Fdn Trust, North East Thames Reg Genet Serv, London, England Univ Queensland, Frazer Inst, Woolloongabba, Qld 4102, AustraliaClement, Emma论文数: 0 引用数: 0 h-index: 0机构: Great Ormond St Hosp Children NHS Fdn Trust, North East Thames Reg Genet Serv, London, England Univ Queensland, Frazer Inst, Woolloongabba, Qld 4102, AustraliaNakou, Vasiliki论文数: 0 引用数: 0 h-index: 0机构: UCL, Great Ormond St Hosp Children NHS Fdn Trust, Paediat Neurol, London, England Univ Queensland, Frazer Inst, Woolloongabba, Qld 4102, Australia论文数: 引用数: h-index:机构:Dobosz, Dominika论文数: 0 引用数: 0 h-index: 0机构: Jagiellonian Univ, Malopolska Ctr Biotechnol, Krakow, Poland Univ Queensland, Frazer Inst, Woolloongabba, Qld 4102, AustraliaKaliakatsos, Marios论文数: 0 引用数: 0 h-index: 0机构: UCL, Great Ormond St Hosp Children NHS Fdn Trust, Paediat Neurol, London, England Univ Queensland, Frazer Inst, Woolloongabba, Qld 4102, Australia论文数: 引用数: h-index:机构:Wainwright, Brandon J.论文数: 0 引用数: 0 h-index: 0机构: Univ Queensland, Frazer Inst, Woolloongabba, Qld 4102, Australia Univ Queensland, Frazer Inst, Woolloongabba, Qld 4102, Australia
- [2] A conserved and essential basic region mediates tRNA binding to the Elp1 subunit of the Saccharomyces cerevisiae Elongator complexMOLECULAR MICROBIOLOGY, 2014, 92 (06) : 1227 - 1242Di Santo, Rachael论文数: 0 引用数: 0 h-index: 0机构: Univ Dundee, Coll Life Sci, Ctr Gene Regulat & Express, Dundee DD1 5EH, Scotland Univ Dundee, Coll Life Sci, Ctr Gene Regulat & Express, Dundee DD1 5EH, ScotlandBandau, Susanne论文数: 0 引用数: 0 h-index: 0机构: Univ Dundee, Coll Life Sci, Ctr Gene Regulat & Express, Dundee DD1 5EH, Scotland Univ Dundee, Coll Life Sci, Ctr Gene Regulat & Express, Dundee DD1 5EH, ScotlandStark, Michael J. R.论文数: 0 引用数: 0 h-index: 0机构: Univ Dundee, Coll Life Sci, Ctr Gene Regulat & Express, Dundee DD1 5EH, Scotland Univ Dundee, Coll Life Sci, Ctr Gene Regulat & Express, Dundee DD1 5EH, Scotland
- [3] UBTF Mutation Causes Complex Phenotype of Neurodegeneration and Severe Epilepsy in ChildhoodNEUROPEDIATRICS, 2019, 50 (01) : 57 - 60论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Sterbova, Katalin论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Motol, V Uvalu 84, Prague 15006 5, Czech Republic Charles Univ Prague, Fac Med 2, Dept Pediat Neurol, Prague, Czech Republic Charles Univ Prague, Fac Med 2, Dept Pediat Neurol, DNA Lab, V Uvalu 84, Prague 15006 5, Czech RepublicHaberlova, Jana论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Motol, V Uvalu 84, Prague 15006 5, Czech Republic Charles Univ Prague, Fac Med 2, Dept Pediat Neurol, Prague, Czech Republic Charles Univ Prague, Fac Med 2, Dept Pediat Neurol, DNA Lab, V Uvalu 84, Prague 15006 5, Czech RepublicVyhnalkova, Emilie论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Motol, V Uvalu 84, Prague 15006 5, Czech Republic Charles Univ Prague, Fac Med 2, Dept Biol & Med Genet, Prague, Czech Republic Charles Univ Prague, Fac Med 2, Dept Pediat Neurol, DNA Lab, V Uvalu 84, Prague 15006 5, Czech RepublicNeupauerova, Jana论文数: 0 引用数: 0 h-index: 0机构: Charles Univ Prague, Fac Med 2, Dept Pediat Neurol, DNA Lab, V Uvalu 84, Prague 15006 5, Czech Republic Univ Hosp Motol, V Uvalu 84, Prague 15006 5, Czech Republic Charles Univ Prague, Fac Med 2, Dept Pediat Neurol, DNA Lab, V Uvalu 84, Prague 15006 5, Czech RepublicStanek, David论文数: 0 引用数: 0 h-index: 0机构: Charles Univ Prague, Fac Med 2, Dept Pediat Neurol, DNA Lab, V Uvalu 84, Prague 15006 5, Czech Republic Univ Hosp Motol, V Uvalu 84, Prague 15006 5, Czech Republic Charles Univ Prague, Fac Med 2, Dept Pediat Neurol, DNA Lab, V Uvalu 84, Prague 15006 5, Czech RepublicSediva, Marie论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Motol, V Uvalu 84, Prague 15006 5, Czech Republic Charles Univ Prague, Fac Med 2, Dept Pediat Neurol, Prague, Czech Republic Charles Univ Prague, Fac Med 2, Dept Pediat Neurol, DNA Lab, V Uvalu 84, Prague 15006 5, Czech Republic论文数: 引用数: h-index:机构:Seeman, Pavel论文数: 0 引用数: 0 h-index: 0机构: Charles Univ Prague, Fac Med 2, Dept Pediat Neurol, DNA Lab, V Uvalu 84, Prague 15006 5, Czech Republic Univ Hosp Motol, V Uvalu 84, Prague 15006 5, Czech Republic Charles Univ Prague, Fac Med 2, Dept Pediat Neurol, DNA Lab, V Uvalu 84, Prague 15006 5, Czech Republic
- [4] A novel LMNA mutation causes severe congenital phenotype with cytoplasmic bodiesNEUROMUSCULAR DISORDERS, 2015, 25 : S279 - S279Nishikawa, A.论文数: 0 引用数: 0 h-index: 0机构: Natl Ctr Neurol & Psychiat, Dept Neuromuscular Res, Tokyo, Japan Natl Ctr Neurol & Psychiat, Dept Neuromuscular Res, Tokyo, JapanMitsuhashi, S.论文数: 0 引用数: 0 h-index: 0机构: Natl Ctr Neurol & Psychiat, Dept Neuromuscular Res, Tokyo, Japan Natl Ctr Neurol & Psychiat, Dept Neuromuscular Res, Tokyo, Japan论文数: 引用数: h-index:机构:Uruha, A.论文数: 0 引用数: 0 h-index: 0机构: Natl Ctr Neurol & Psychiat, Dept Neuromuscular Res, Tokyo, Japan Natl Ctr Neurol & Psychiat, Dept Neuromuscular Res, Tokyo, JapanNoguchi, S.论文数: 0 引用数: 0 h-index: 0机构: Natl Ctr Neurol & Psychiat, Dept Neuromuscular Res, Tokyo, Japan Natl Ctr Neurol & Psychiat, Dept Neuromuscular Res, Tokyo, JapanNishino, I.论文数: 0 引用数: 0 h-index: 0机构: Natl Ctr Neurol & Psychiat, Dept Neuromuscular Res, Tokyo, Japan Natl Ctr Neurol & Psychiat, Dept Neuromuscular Res, Tokyo, Japan
- [5] Complete loss of function of the ubiquitin ligase HERC2 causes a severe neurodevelopmental phenotypeEuropean Journal of Human Genetics, 2017, 25 : 52 - 58Fanny Morice-Picard论文数: 0 引用数: 0 h-index: 0机构: Univ. Bordeaux,Giovanni Benard论文数: 0 引用数: 0 h-index: 0机构: Univ. Bordeaux,Hamid R Rezvani论文数: 0 引用数: 0 h-index: 0机构: Univ. Bordeaux,Eulalie Lasseaux论文数: 0 引用数: 0 h-index: 0机构: Univ. Bordeaux,Delphine Simon论文数: 0 引用数: 0 h-index: 0机构: Univ. Bordeaux,Sébastien Moutton论文数: 0 引用数: 0 h-index: 0机构: Univ. Bordeaux,Caroline Rooryck论文数: 0 引用数: 0 h-index: 0机构: Univ. Bordeaux,Didier Lacombe论文数: 0 引用数: 0 h-index: 0机构: Univ. Bordeaux,Clarisse Baumann论文数: 0 引用数: 0 h-index: 0机构: Univ. Bordeaux,Benoit Arveiler论文数: 0 引用数: 0 h-index: 0机构: Univ. Bordeaux,
- [6] Complete loss of function of the ubiquitin ligase HERC2 causes a severe neurodevelopmental phenotypeEUROPEAN JOURNAL OF HUMAN GENETICS, 2017, 25 (01) : 52 - 58论文数: 引用数: h-index:机构:Benard, Giovanni论文数: 0 引用数: 0 h-index: 0机构: Univ Bordeaux, MRGM EA4576, Bordeaux, France Univ Bordeaux, MRGM EA4576, Bordeaux, FranceRezvani, Hamid R.论文数: 0 引用数: 0 h-index: 0机构: INSERM, Biotherapies Malad Genet & Canc, Bordeaux, France Univ Bordeaux, MRGM EA4576, Bordeaux, FranceLasseaux, Eulalie论文数: 0 引用数: 0 h-index: 0机构: CHU Bordeaux, Serv Genet Med, Bordeaux, France Univ Bordeaux, MRGM EA4576, Bordeaux, FranceSimon, Delphine论文数: 0 引用数: 0 h-index: 0机构: Univ Bordeaux, MRGM EA4576, Bordeaux, France Univ Bordeaux, MRGM EA4576, Bordeaux, FranceMoutton, Sebastien论文数: 0 引用数: 0 h-index: 0机构: Univ Bordeaux, MRGM EA4576, Bordeaux, France Univ Bordeaux, MRGM EA4576, Bordeaux, FranceRooryck, Caroline论文数: 0 引用数: 0 h-index: 0机构: Univ Bordeaux, MRGM EA4576, Bordeaux, France CHU Bordeaux, Serv Genet Med, Bordeaux, France Univ Bordeaux, MRGM EA4576, Bordeaux, France论文数: 引用数: h-index:机构:Baumann, Clarisse论文数: 0 引用数: 0 h-index: 0机构: Hop Robert Debre, Serv Genet Med, Paris, France Univ Bordeaux, MRGM EA4576, Bordeaux, France论文数: 引用数: h-index:机构:
- [7] Lesch-Nyhan syndrome: a novel complex mutation with severe phenotypeCLINICAL GENETICS, 2010, 78 (03) : 296 - 297Gucev, Z.论文数: 0 引用数: 0 h-index: 0机构: Univ Skopje, Skopje 1000, Macedonia Univ Skopje, Skopje 1000, MacedoniaKoceva, S.论文数: 0 引用数: 0 h-index: 0机构: Univ Skopje, Skopje 1000, Macedonia Univ Skopje, Skopje 1000, MacedoniaMarinaki, A.论文数: 0 引用数: 0 h-index: 0机构: St Thomas Hosp, Purine Res Lab, GSTS Pathol, London, England Univ Skopje, Skopje 1000, MacedoniaFairbanks, L.论文数: 0 引用数: 0 h-index: 0机构: St Thomas Hosp, Purine Res Lab, GSTS Pathol, London, England Univ Skopje, Skopje 1000, MacedoniaKirovski, I.论文数: 0 引用数: 0 h-index: 0机构: Univ Skopje, Skopje 1000, Macedonia Univ Skopje, Skopje 1000, MacedoniaTasic, V.论文数: 0 引用数: 0 h-index: 0机构: Univ Skopje, Skopje 1000, Macedonia Univ Skopje, Skopje 1000, Macedonia
- [8] A novel mutation in DNAJB6 causes a more severe phenotype and greater loss of anti-aggregation functionNEUROMUSCULAR DISORDERS, 2014, 24 (9-10) : 902 - 902Jonson, P. H.论文数: 0 引用数: 0 h-index: 0机构: Univ Helsinki, Folkhalsan Inst Genet, Helsinki, Finland Univ Helsinki, Haartman Inst, Helsinki, Finland Univ Helsinki, Folkhalsan Inst Genet, Helsinki, FinlandPalmio, J.论文数: 0 引用数: 0 h-index: 0机构: Tampere Univ Hosp, Dept Neurol, Neuromuscular Res Unit, Tampere, Finland Univ Tampere, FIN-33101 Tampere, Finland Univ Helsinki, Folkhalsan Inst Genet, Helsinki, Finland论文数: 引用数: h-index:机构:Luque, H.论文数: 0 引用数: 0 h-index: 0机构: Univ Helsinki, Folkhalsan Inst Genet, Helsinki, Finland Univ Helsinki, Haartman Inst, Helsinki, Finland Univ Helsinki, Folkhalsan Inst Genet, Helsinki, FinlandUdd, B.论文数: 0 引用数: 0 h-index: 0机构: Univ Helsinki, Folkhalsan Inst Genet, Helsinki, Finland Univ Helsinki, Haartman Inst, Helsinki, Finland Univ Helsinki, Folkhalsan Inst Genet, Helsinki, Finland
- [9] A novel mutation in SPART gene causes a severe neurodevelopmental delay due to mitochondrial dysfunction with complex I impairments and altered pyruvate metabolismFASEB JOURNAL, 2019, 33 (10): : 11284 - 11302Diquigiovanni, Chiara论文数: 0 引用数: 0 h-index: 0机构: Univ Bologna, St Orsola Malpighi Hosp, Dept Med & Surg Sci DIMEC, Bologna, Italy Univ Bologna, St Orsola Malpighi Hosp, Dept Med & Surg Sci DIMEC, Bologna, ItalyBergamini, Christian论文数: 0 引用数: 0 h-index: 0机构: Univ Bologna, St Orsola Malpighi Hosp, Dept Pharm & Biotechnol FaBit, Bologna, Italy Univ Bologna, St Orsola Malpighi Hosp, Dept Med & Surg Sci DIMEC, Bologna, ItalyDiaz, Rebeca论文数: 0 引用数: 0 h-index: 0机构: Univ St Andrews, Sch Med, St Andrews, Fife, Scotland Univ Bologna, St Orsola Malpighi Hosp, Dept Med & Surg Sci DIMEC, Bologna, ItalyLiparulo, Irene论文数: 0 引用数: 0 h-index: 0机构: Univ Bologna, St Orsola Malpighi Hosp, Dept Pharm & Biotechnol FaBit, Bologna, Italy Univ Bologna, St Orsola Malpighi Hosp, Dept Med & Surg Sci DIMEC, Bologna, ItalyBianco, Francesca论文数: 0 引用数: 0 h-index: 0机构: Univ Bologna, St Orsola Malpighi Hosp, Dept Med & Surg Sci DIMEC, Bologna, Italy Univ Bologna, St Orsola Malpighi Hosp, Dept Med & Surg Sci DIMEC, Bologna, ItalyMasin, Luca论文数: 0 引用数: 0 h-index: 0机构: Univ Bologna, St Orsola Malpighi Hosp, Dept Pharm & Biotechnol FaBit, Bologna, Italy Univ Bologna, St Orsola Malpighi Hosp, Dept Med & Surg Sci DIMEC, Bologna, ItalyBaldassarro, Vito Antonio论文数: 0 引用数: 0 h-index: 0机构: IRET Fdn, Bologna, Italy Univ Bologna, St Orsola Malpighi Hosp, Dept Med & Surg Sci DIMEC, Bologna, ItalyRizzardi, Nicola论文数: 0 引用数: 0 h-index: 0机构: Univ Bologna, St Orsola Malpighi Hosp, Dept Med & Surg Sci DIMEC, Bologna, Italy Univ Bologna, St Orsola Malpighi Hosp, Dept Med & Surg Sci DIMEC, Bologna, ItalyTranchina, Antonia论文数: 0 引用数: 0 h-index: 0机构: Univ Bologna, St Orsola Malpighi Hosp, Dept Pharm & Biotechnol FaBit, Bologna, Italy Univ Bologna, St Orsola Malpighi Hosp, Dept Med & Surg Sci DIMEC, Bologna, ItalyBuscherini, Francesco论文数: 0 引用数: 0 h-index: 0机构: Univ Bologna, St Orsola Malpighi Hosp, Dept Med & Surg Sci DIMEC, Bologna, Italy Univ Bologna, St Orsola Malpighi Hosp, Dept Med & Surg Sci DIMEC, Bologna, ItalyWischmeijer, Anita论文数: 0 引用数: 0 h-index: 0机构: Reg Hosp South Tyrol, Dept Pediat, Clin Genet Serv, Bolzano, Italy Univ Bologna, St Orsola Malpighi Hosp, Dept Med & Surg Sci DIMEC, Bologna, ItalyPippucci, Tommaso论文数: 0 引用数: 0 h-index: 0机构: Univ Bologna, St Orsola Malpighi Hosp, Dept Med & Surg Sci DIMEC, Bologna, Italy Univ Bologna, St Orsola Malpighi Hosp, Dept Med & Surg Sci DIMEC, Bologna, ItalyScarano, Emanuela论文数: 0 引用数: 0 h-index: 0机构: Univ Bologna, Rare Dis Unit, Dept Pediat, St Orsola Malpighi Hosp, Bologna, Italy Univ Bologna, St Orsola Malpighi Hosp, Dept Med & Surg Sci DIMEC, Bologna, Italy论文数: 引用数: h-index:机构:Fato, Romana论文数: 0 引用数: 0 h-index: 0机构: Univ Bologna, St Orsola Malpighi Hosp, Dept Pharm & Biotechnol FaBit, Bologna, Italy Univ Bologna, St Orsola Malpighi Hosp, Dept Med & Surg Sci DIMEC, Bologna, Italy论文数: 引用数: h-index:机构:Paracchini, Silvia论文数: 0 引用数: 0 h-index: 0机构: Univ St Andrews, Sch Med, St Andrews, Fife, Scotland Univ Bologna, St Orsola Malpighi Hosp, Dept Med & Surg Sci DIMEC, Bologna, ItalyBonora, Elena论文数: 0 引用数: 0 h-index: 0机构: Univ Bologna, St Orsola Malpighi Hosp, Dept Med & Surg Sci DIMEC, Bologna, Italy Univ Bologna, St Orsola Malpighi Hosp, Dept Med & Surg Sci DIMEC, Bologna, Italy
- [10] Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorderGENETICS IN MEDICINE, 2024, 26 (09)Kohler, Jennefer N.论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USA Stanford Univ, Sch Med, Dept Pediat, Div Med Genet, Stanford, CA USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USALegro, Nicole R.论文数: 0 引用数: 0 h-index: 0机构: MedStar Washington Hosp Ctr, Dept Obstet & Gynecol, Washington, DC 20007 USA Georgetown Univ Hosp, Washington, DC USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USABaldridge, Dustin论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Sch Med, Model Organism Screening Ctr, Dept Dev Biol, St Louis, MO USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USAShin, Jimann论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Sch Med, Model Organism Screening Ctr, Dept Dev Biol, St Louis, MO USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USABowman, Angela论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Sch Med, Model Organism Screening Ctr, Dept Dev Biol, St Louis, MO USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USAUgur, Berrak论文数: 0 引用数: 0 h-index: 0机构: Yale Univ, Sch Med, Dept Neurosci, New Haven, CT USA Yale Univ, Sch Med, Dept Cell Biol, New Haven, CT USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USAJackstadt, Madelyn M.论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Dept Chem, St Louis, MO USA Washington Univ, Dept Med, St Louis, MO USA Washington Univ, Ctr Prote Metabol & Isotope Tracing, St Louis, MO USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USAShriver, Leah P.论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Dept Chem, St Louis, MO USA Washington Univ, Dept Med, St Louis, MO USA Washington Univ, Ctr Prote Metabol & Isotope Tracing, St Louis, MO USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USAPatti, Gary J.论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Dept Chem, St Louis, MO USA Washington Univ, Dept Med, St Louis, MO USA Washington Univ, Ctr Prote Metabol & Isotope Tracing, St Louis, MO USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USAZhang, Bo论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Sch Med, Model Organism Screening Ctr, Dept Dev Biol, St Louis, MO USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USAFeng, Wenjia论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Sch Med, Model Organism Screening Ctr, Dept Dev Biol, St Louis, MO USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USAMcAdow, Anthony R.论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Sch Med, Model Organism Screening Ctr, Dept Dev Biol, St Louis, MO USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USAGoddard, Page论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Sch Med, Dept Genet, Stanford, CA USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USAUngar, Rachel A.论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Sch Med, Dept Genet, Stanford, CA USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USAJensen, Tanner论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Sch Med, Dept Genet, Stanford, CA USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USASmith, Kevin S.论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Sch Med, Dept Pathol, Stanford, CA USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USAFresard, Laure论文数: 0 引用数: 0 h-index: 0机构: Invitae, San Francisco, CA USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USAAlvarez, Raquel论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USA Stanford Univ, Sch Med, Div Cardiovasc Med, Stanford, CA USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USABonner, Devon论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USA Stanford Univ, Sch Med, Dept Pediat, Div Med Genet, Stanford, CA USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USAReuter, Chloe M.论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USA Stanford Univ, Sch Med, Dept Pediat, Div Med Genet, Stanford, CA USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USAMcCormack, Colleen论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USAKravets, Elijah论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USAMarwaha, Shruti论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USAHolt, James M.论文数: 0 引用数: 0 h-index: 0机构: PacBio, 1305 OBrien Dr, Menlo Pk, CA USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USAWorthey, Elizabeth A.论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USA Univ Alabama Birmingham, Ctr Computat Genom & Data Sci, Dept Genet, Birmingham, AL USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USAAshley, Euan A.论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Sch Med, Div Cardiovasc Med, Stanford, CA USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USAMontgomery, Stephen B.论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Sch Med, Dept Genet, Stanford, CA USA Stanford Univ, Sch Med, Dept Pathol, Stanford, CA USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USAFisher, Paul G.论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USA Stanford Univ, Sch Med, Dept Pediat, Div Neurol & Neurol Sci, Stanford, CA USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USAPostlethwait, John论文数: 0 引用数: 0 h-index: 0机构: Univ Oregon, Inst Neurosci, Eugene, OR USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USADe Camilli, Pietro论文数: 0 引用数: 0 h-index: 0机构: Yale Univ, Howard Hughes Med Inst, Sch Med, Dept Neurosci,Program Cellular Neurosci Neurodegen, New Haven, CT USA Yale Univ, Howard Hughes Med Inst, Sch Med, Dept Cell Biol,Program Cellular Neurosci Neurodege, New Haven, CT USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USASolnica-Krezel, Lila论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Sch Med, Model Organism Screening Ctr, Dept Dev Biol, St Louis, MO USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USABernstein, Jonathan A.论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USA Stanford Univ, Sch Med, Dept Pediat, Div Med Genet, Stanford, CA USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USAWheeler, Matthew T.论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USA Stanford Univ, Sch Med, Div Cardiovasc Med, Stanford, CA USA Stanford Univ, Stanford Ctr Undiagnosed Dis, Stanford, CA USA