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- [41] Novel recessive and dominant mutations in collagen VI causing Ullrich congenital muscular dystrophy and correlation with mRNA degradationNEUROMUSCULAR DISORDERS, 2007, 17 (9-10) : 848 - 849Brinas, L.论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 06, IFRI4, Inst Myol, INSERM U582 UMR S582, Paris, France Univ Paris 06, IFRI4, Inst Myol, INSERM U582 UMR S582, Paris, France论文数: 引用数: h-index:机构:Ledeuil, C.论文数: 0 引用数: 0 h-index: 0机构: Grp Hosp Pitie Salpetriere, APHP, UF Cardiogenet Myogenet, Serv Biochim Metabol, F-75634 Paris, France Univ Paris 06, IFRI4, Inst Myol, INSERM U582 UMR S582, Paris, FranceQuijano-Roy, S.论文数: 0 引用数: 0 h-index: 0机构: Hop Raymond Poincare, APHP, Serv Pediat, Garches, France Etab Hosp Special Ali Ait Idir, Algiers, Algeria Univ Paris 06, IFRI4, Inst Myol, INSERM U582 UMR S582, Paris, FranceMakri, S.论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 06, IFRI4, Inst Myol, INSERM U582 UMR S582, Paris, FranceMerlini, L.论文数: 0 引用数: 0 h-index: 0机构: Ist Ortoped Rizzoli, Neuromusc Unit, Bologna, Italy Univ Paris 06, IFRI4, Inst Myol, INSERM U582 UMR S582, Paris, FranceTopaloglu, H.论文数: 0 引用数: 0 h-index: 0机构: Hacettepe Childrens Hosp Med Ctr, Dept Paediat, Neurol Sect, Ankara, Turkey Univ Paris 06, IFRI4, Inst Myol, INSERM U582 UMR S582, Paris, FranceRoelens, F.论文数: 0 引用数: 0 h-index: 0机构: Dominiek Savio Inst, Gits, Belgium Univ Paris 06, IFRI4, Inst Myol, INSERM U582 UMR S582, Paris, FranceHovers, V.论文数: 0 引用数: 0 h-index: 0机构: Acad Hosp Maastricht, Maastricht, Netherlands Univ Paris 06, IFRI4, Inst Myol, INSERM U582 UMR S582, Paris, FranceJeannet, P.论文数: 0 引用数: 0 h-index: 0机构: CHUV BHII, Neuropaediat Unit, Lausanne, Switzerland Univ Paris 06, IFRI4, Inst Myol, INSERM U582 UMR S582, Paris, FranceEstournet, B.论文数: 0 引用数: 0 h-index: 0机构: Hop Raymond Poincare, APHP, Serv Pediat, Garches, France Univ Paris 06, IFRI4, Inst Myol, INSERM U582 UMR S582, Paris, FranceRichard, P.论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 06, Grp Hosp Pitie Salpetriere, UF Cardiogenet Myogen, INSERM U582 UMR S582 IFRI4 APHP, Paris, France Univ Paris 06, IFRI4, Inst Myol, INSERM U582 UMR S582, Paris, FranceGuicheney, P.论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 06, IFRI4, Inst Myol, INSERM U582 UMR S582, Paris, France Univ Paris 06, IFRI4, Inst Myol, INSERM U582 UMR S582, Paris, FranceAllamand, V.论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 06, IFRI4, Inst Myol, INSERM U582 UMR S582, Paris, France Univ Paris 06, IFRI4, Inst Myol, INSERM U582 UMR S582, Paris, France
- [42] Skipping of exon 16 in COL6A3 is a recurrent mutation causing severe congenital muscular dystrophy type UllrichNEUROMUSCULAR DISORDERS, 2007, 17 (9-10) : 844 - 844Zou, Y.论文数: 0 引用数: 0 h-index: 0机构: Univ Penn, Sch Med, Childrens Hosp Philadelphia, Div Neurol, Philadelphia, PA 19104 USA Univ Penn, Sch Med, Childrens Hosp Philadelphia, Div Neurol, Philadelphia, PA 19104 USASchessl, J.论文数: 0 引用数: 0 h-index: 0机构: Univ Penn, Sch Med, Childrens Hosp Philadelphia, Div Neurol, Philadelphia, PA 19104 USA Univ Penn, Sch Med, Childrens Hosp Philadelphia, Div Neurol, Philadelphia, PA 19104 USALampe, A.论文数: 0 引用数: 0 h-index: 0机构: Univ Newcastle Upon Tyne, Ctr Int Life, Inst Human Genet, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England Univ Penn, Sch Med, Childrens Hosp Philadelphia, Div Neurol, Philadelphia, PA 19104 USAHu, Y.论文数: 0 引用数: 0 h-index: 0机构: Univ Penn, Sch Med, Childrens Hosp Philadelphia, Div Neurol, Philadelphia, PA 19104 USA Univ Penn, Sch Med, Childrens Hosp Philadelphia, Div Neurol, Philadelphia, PA 19104 USAJimenez-Mallebrera, C.论文数: 0 引用数: 0 h-index: 0机构: Univ London Imperial Coll Sci & Technol, Hammersmith Hosp, Dubowitz Neuromusc Ctr, London, England Univ Penn, Sch Med, Childrens Hosp Philadelphia, Div Neurol, Philadelphia, PA 19104 USASchreiber, G.论文数: 0 引用数: 0 h-index: 0机构: Hosp Kassel, Dept Neuropediat, Kassel, Germany Univ Penn, Sch Med, Childrens Hosp Philadelphia, Div Neurol, Philadelphia, PA 19104 USAStolte-Dijkstra, I.论文数: 0 引用数: 0 h-index: 0机构: Univ Groningen, Med Ctr, Groningen, Netherlands Univ Penn, Sch Med, Childrens Hosp Philadelphia, Div Neurol, Philadelphia, PA 19104 USAFock, A.论文数: 0 引用数: 0 h-index: 0机构: Univ Groningen, Med Ctr, Groningen, Netherlands Univ Penn, Sch Med, Childrens Hosp Philadelphia, Div Neurol, Philadelphia, PA 19104 USAChu, M.论文数: 0 引用数: 0 h-index: 0机构: Thomas Jefferson Univ, Jefferson Inst Mol Med, Dept Dermatol & Cutaneous Biol, Philadelphia, PA 19107 USA Univ Penn, Sch Med, Childrens Hosp Philadelphia, Div Neurol, Philadelphia, PA 19104 USABushby, K.论文数: 0 引用数: 0 h-index: 0机构: Univ Newcastle Upon Tyne, Ctr Int Life, Inst Human Genet, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England Univ Penn, Sch Med, Childrens Hosp Philadelphia, Div Neurol, Philadelphia, PA 19104 USAWeiss, R.论文数: 0 引用数: 0 h-index: 0机构: Univ Utah, Dept Human Genet, Salt Lake City, UT USA Univ Penn, Sch Med, Childrens Hosp Philadelphia, Div Neurol, Philadelphia, PA 19104 USAFlanigan, K.论文数: 0 引用数: 0 h-index: 0机构: Univ Utah, Dept Human Genet, Salt Lake City, UT USA Univ Penn, Sch Med, Childrens Hosp Philadelphia, Div Neurol, Philadelphia, PA 19104 USAMuntoni, F.论文数: 0 引用数: 0 h-index: 0机构: Univ London Imperial Coll Sci & Technol, Hammersmith Hosp, Dubowitz Neuromusc Ctr, London, England Univ Penn, Sch Med, Childrens Hosp Philadelphia, Div Neurol, Philadelphia, PA 19104 USABoennemann, C.论文数: 0 引用数: 0 h-index: 0机构: Univ Penn, Sch Med, Childrens Hosp Philadelphia, Div Neurol, Philadelphia, PA 19104 USA Univ Penn, Sch Med, Childrens Hosp Philadelphia, Div Neurol, Philadelphia, PA 19104 USA
- [43] Ullrich Congenital Muscular Dystrophy Possibly Related With COL6A1 p.Gly302Arg VariantANNALS OF REHABILITATION MEDICINE-ARM, 2014, 38 (02): : 292 - 296Park, Yoonhong论文数: 0 引用数: 0 h-index: 0机构: Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Phys & Rehabil Med, 81 Irwon Ro, Seoul 135710, South Korea Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Phys & Rehabil Med, 81 Irwon Ro, Seoul 135710, South KoreaPark, Myung Seok论文数: 0 引用数: 0 h-index: 0机构: Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Phys & Rehabil Med, 81 Irwon Ro, Seoul 135710, South Korea Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Phys & Rehabil Med, 81 Irwon Ro, Seoul 135710, South KoreaSung, Duk Hyun论文数: 0 引用数: 0 h-index: 0机构: Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Phys & Rehabil Med, 81 Irwon Ro, Seoul 135710, South Korea Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Phys & Rehabil Med, 81 Irwon Ro, Seoul 135710, South KoreaSohn, Ji Yeon论文数: 0 引用数: 0 h-index: 0机构: Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Lab Med & Genet, Seoul, South Korea Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Phys & Rehabil Med, 81 Irwon Ro, Seoul 135710, South KoreaKi, Chang-Seok论文数: 0 引用数: 0 h-index: 0机构: Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Lab Med & Genet, Seoul, South Korea Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Phys & Rehabil Med, 81 Irwon Ro, Seoul 135710, South KoreaKim, Du-Hwan论文数: 0 引用数: 0 h-index: 0机构: Keimyung Univ, Dongsan Med Ctr, Dept Phys & Rehabil Med, Daegu, South Korea Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Phys & Rehabil Med, 81 Irwon Ro, Seoul 135710, South Korea
- [44] Identification of Two Novel LAMA2 Mutations in a Chinese Patient with Congenital Muscular DystrophyFRONTIERS IN GENETICS, 2018, 9Zhou, Jing论文数: 0 引用数: 0 h-index: 0机构: Nanjing Med Univ, Nanjing Matern & Child Hlth Care Hosp, Affiliated Obstet & Gynecol Hosp, State Key Lab Reprod Med,Dept Prenatal Diag, Nanjing, Jiangsu, Peoples R China Nanjing Med Univ, Nanjing Matern & Child Hlth Care Hosp, Affiliated Obstet & Gynecol Hosp, State Key Lab Reprod Med,Dept Prenatal Diag, Nanjing, Jiangsu, Peoples R ChinaTan, Jianxin论文数: 0 引用数: 0 h-index: 0机构: Nanjing Med Univ, Nanjing Matern & Child Hlth Care Hosp, Affiliated Obstet & Gynecol Hosp, State Key Lab Reprod Med,Dept Prenatal Diag, Nanjing, Jiangsu, Peoples R China Nanjing Med Univ, Nanjing Matern & Child Hlth Care Hosp, Affiliated Obstet & Gynecol Hosp, State Key Lab Reprod Med,Dept Prenatal Diag, Nanjing, Jiangsu, Peoples R ChinaMa, Dingyuan论文数: 0 引用数: 0 h-index: 0机构: Nanjing Med Univ, Nanjing Matern & Child Hlth Care Hosp, Affiliated Obstet & Gynecol Hosp, State Key Lab Reprod Med,Dept Prenatal Diag, Nanjing, Jiangsu, Peoples R China Nanjing Med Univ, Nanjing Matern & Child Hlth Care Hosp, Affiliated Obstet & Gynecol Hosp, State Key Lab Reprod Med,Dept Prenatal Diag, Nanjing, Jiangsu, Peoples R ChinaZhang, Jingjing论文数: 0 引用数: 0 h-index: 0机构: Nanjing Med Univ, Nanjing Matern & Child Hlth Care Hosp, Affiliated Obstet & Gynecol Hosp, State Key Lab Reprod Med,Dept Prenatal Diag, Nanjing, Jiangsu, Peoples R China Nanjing Med Univ, Nanjing Matern & Child Hlth Care Hosp, Affiliated Obstet & Gynecol Hosp, State Key Lab Reprod Med,Dept Prenatal Diag, Nanjing, Jiangsu, Peoples R ChinaCheng, Jian论文数: 0 引用数: 0 h-index: 0机构: Nanjing Med Univ, Nanjing Matern & Child Hlth Care Hosp, Affiliated Obstet & Gynecol Hosp, State Key Lab Reprod Med,Dept Prenatal Diag, Nanjing, Jiangsu, Peoples R China Nanjing Med Univ, Nanjing Matern & Child Hlth Care Hosp, Affiliated Obstet & Gynecol Hosp, State Key Lab Reprod Med,Dept Prenatal Diag, Nanjing, Jiangsu, Peoples R ChinaLuo, Chunyu论文数: 0 引用数: 0 h-index: 0机构: Nanjing Med Univ, Nanjing Matern & Child Hlth Care Hosp, Affiliated Obstet & Gynecol Hosp, State Key Lab Reprod Med,Dept Prenatal Diag, Nanjing, Jiangsu, Peoples R China Nanjing Med Univ, Nanjing Matern & Child Hlth Care Hosp, Affiliated Obstet & Gynecol Hosp, State Key Lab Reprod Med,Dept Prenatal Diag, Nanjing, Jiangsu, Peoples R ChinaLiu, Gang论文数: 0 引用数: 0 h-index: 0机构: Nanjing Med Univ, Nanjing Matern & Child Hlth Care Hosp, Affiliated Obstet & Gynecol Hosp, State Key Lab Reprod Med,Dept Prenatal Diag, Nanjing, Jiangsu, Peoples R China Nanjing Med Univ, Nanjing Matern & Child Hlth Care Hosp, Affiliated Obstet & Gynecol Hosp, State Key Lab Reprod Med,Dept Prenatal Diag, Nanjing, Jiangsu, Peoples R ChinaWang, Yuguo论文数: 0 引用数: 0 h-index: 0机构: Nanjing Med Univ, Nanjing Matern & Child Hlth Care Hosp, Affiliated Obstet & Gynecol Hosp, State Key Lab Reprod Med,Dept Prenatal Diag, Nanjing, Jiangsu, Peoples R China Nanjing Med Univ, Nanjing Matern & Child Hlth Care Hosp, Affiliated Obstet & Gynecol Hosp, State Key Lab Reprod Med,Dept Prenatal Diag, Nanjing, Jiangsu, Peoples R ChinaXu, Zhengfeng论文数: 0 引用数: 0 h-index: 0机构: Nanjing Med Univ, Nanjing Matern & Child Hlth Care Hosp, Affiliated Obstet & Gynecol Hosp, State Key Lab Reprod Med,Dept Prenatal Diag, Nanjing, Jiangsu, Peoples R China Nanjing Med Univ, Nanjing Matern & Child Hlth Care Hosp, Affiliated Obstet & Gynecol Hosp, State Key Lab Reprod Med,Dept Prenatal Diag, Nanjing, Jiangsu, Peoples R China
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- [49] Gapmer antisense oligonucleotides selectively suppress the mutant allele of COL6A3 gene in dominant Ullrich congenital muscular dystrophyNEUROMUSCULAR DISORDERS, 2017, 27 : S107 - S107Zhou, H.论文数: 0 引用数: 0 h-index: 0机构: UCL, London, England UCL, London, EnglandMarrosu, E.论文数: 0 引用数: 0 h-index: 0机构: UCL, London, England UCL, London, EnglandAla, P.论文数: 0 引用数: 0 h-index: 0机构: UCL, London, England UCL, London, EnglandMuntoni, F.论文数: 0 引用数: 0 h-index: 0机构: UCL, London, England UCL, London, England
- [50] Characterization of a rare case of Ullrich congenital muscular dystrophy due to truncating mutations within the COL6A1 gene C-Terminal domain: a case reportBMC MEDICAL GENETICS, 2013, 14Martoni, Elena论文数: 0 引用数: 0 h-index: 0机构: Univ Ferrara, Med Genet Sect, Dept Med Sci, I-44100 Ferrara, Italy Univ Ferrara, Med Genet Sect, Dept Med Sci, I-44100 Ferrara, ItalyPetrini, Stefania论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Pediat Hosp, Dept Neurosci, Unit Muscular & Neurodegenerat Disorders, Rome, Italy Univ Ferrara, Med Genet Sect, Dept Med Sci, I-44100 Ferrara, ItalyTrabanelli, Cecilia论文数: 0 引用数: 0 h-index: 0机构: Univ Ferrara, Med Genet Sect, Dept Med Sci, I-44100 Ferrara, Italy Univ Ferrara, Med Genet Sect, Dept Med Sci, I-44100 Ferrara, ItalySabatelli, Patrizia论文数: 0 引用数: 0 h-index: 0机构: IOR, Unit Bologna, IGM CNR, Bologna, Italy Univ Ferrara, Med Genet Sect, Dept Med Sci, I-44100 Ferrara, Italy论文数: 引用数: h-index:机构:Selvatici, Rita论文数: 0 引用数: 0 h-index: 0机构: Univ Ferrara, Med Genet Sect, Dept Med Sci, I-44100 Ferrara, Italy Univ Ferrara, Med Genet Sect, Dept Med Sci, I-44100 Ferrara, ItalyD'Amico, Adele论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Pediat Hosp, Dept Neurosci, Unit Muscular & Neurodegenerat Disorders, Rome, Italy Univ Ferrara, Med Genet Sect, Dept Med Sci, I-44100 Ferrara, ItalyFalzarano, Sofia论文数: 0 引用数: 0 h-index: 0机构: Univ Ferrara, Med Genet Sect, Dept Med Sci, I-44100 Ferrara, Italy Univ Ferrara, Med Genet Sect, Dept Med Sci, I-44100 Ferrara, ItalyBertini, Enrico论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Pediat Hosp, Dept Neurosci, Unit Muscular & Neurodegenerat Disorders, Rome, Italy Univ Ferrara, Med Genet Sect, Dept Med Sci, I-44100 Ferrara, Italy论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构: