共 50 条
- [21] Effect on collagen VI extra-cellular assembly of COL6A1 and COL6A2 C-terminal mutations in Ullrich congenital muscular dystrophyNEUROMUSCULAR DISORDERS, 2006, 16 (9-10) : 714 - 714Sabatelli, P.论文数: 0 引用数: 0 h-index: 0机构: Ist Ortoped Rizzoli, CNR, ITOI, Bologna, ItalyZou, Y.论文数: 0 引用数: 0 h-index: 0机构: Ist Ortoped Rizzoli, CNR, ITOI, Bologna, ItalySquarzoni, S.论文数: 0 引用数: 0 h-index: 0机构: Ist Ortoped Rizzoli, CNR, ITOI, Bologna, ItalyBoennemann, C.论文数: 0 引用数: 0 h-index: 0机构: Ist Ortoped Rizzoli, CNR, ITOI, Bologna, ItalyMerlini, L.论文数: 0 引用数: 0 h-index: 0机构: Ist Ortoped Rizzoli, CNR, ITOI, Bologna, ItalyPepe, G.论文数: 0 引用数: 0 h-index: 0机构: Ist Ortoped Rizzoli, CNR, ITOI, Bologna, ItalyGiusti, B.论文数: 0 引用数: 0 h-index: 0机构: Ist Ortoped Rizzoli, CNR, ITOI, Bologna, ItalyPetrini, S.论文数: 0 引用数: 0 h-index: 0机构: Ist Ortoped Rizzoli, CNR, ITOI, Bologna, ItalyBertini, E.论文数: 0 引用数: 0 h-index: 0机构: Ist Ortoped Rizzoli, CNR, ITOI, Bologna, ItalySudano, D.论文数: 0 引用数: 0 h-index: 0机构: Ist Ortoped Rizzoli, CNR, ITOI, Bologna, ItalyChu, M. L.论文数: 0 引用数: 0 h-index: 0机构: Ist Ortoped Rizzoli, CNR, ITOI, Bologna, ItalyMaraldi, N. M.论文数: 0 引用数: 0 h-index: 0机构: Ist Ortoped Rizzoli, CNR, ITOI, Bologna, Italy
- [22] Gene expression and proteome profiles in Col6a1-/- mice, a model of Ullrich congenital muscular dystrophy (UCMD)NEUROMUSCULAR DISORDERS, 2009, 19 (8-9) : 630 - 630Bovolenta, M.论文数: 0 引用数: 0 h-index: 0机构: Univ Ferrara, I-44100 Ferrara, Italy Univ Ferrara, I-44100 Ferrara, ItalyDe Palma, S.论文数: 0 引用数: 0 h-index: 0机构: CNR, I-20133 Milan, Italy Univ Ferrara, I-44100 Ferrara, ItalyVasso, M.论文数: 0 引用数: 0 h-index: 0机构: Univ Ferrara, I-44100 Ferrara, Italy Univ Ferrara, I-44100 Ferrara, ItalyMaraldi, N. M.论文数: 0 引用数: 0 h-index: 0机构: CNR, IGM, I-40126 Bologna, Italy Univ Ferrara, I-44100 Ferrara, Italy论文数: 引用数: h-index:机构:Merlini, L.论文数: 0 引用数: 0 h-index: 0机构: Univ Ferrara, I-44100 Ferrara, Italy Univ Ferrara, I-44100 Ferrara, ItalySabatelli, P.论文数: 0 引用数: 0 h-index: 0机构: Univ Ferrara, I-44100 Ferrara, Italy Univ Ferrara, I-44100 Ferrara, ItalyTiepolo, T.论文数: 0 引用数: 0 h-index: 0机构: Univ Padua, Padua, Italy Univ Ferrara, I-44100 Ferrara, Italy论文数: 引用数: h-index:机构:Bernardi, P.论文数: 0 引用数: 0 h-index: 0机构: Univ Padua, Padua, Italy Univ Ferrara, I-44100 Ferrara, ItalyGelfi, C.论文数: 0 引用数: 0 h-index: 0机构: CNR, I-20133 Milan, Italy Univ Ferrara, I-44100 Ferrara, Italy论文数: 引用数: h-index:机构:
- [23] CRISPR/Cas9 Allele-Specific Design to Inactivate A Dominant Negative Mutation in COL6A1 Causing Ullrich Muscular DystrophyMOLECULAR THERAPY, 2022, 30 (04) : 91 - 91Benati, Daniela论文数: 0 引用数: 0 h-index: 0机构: Univ Modena & Reggio Emilia, Dept Life Sci, Modena, Italy Univ Modena & Reggio Emilia, Dept Life Sci, Modena, ItalyPatrizi, Clarissa论文数: 0 引用数: 0 h-index: 0机构: Univ Modena & Reggio Emilia, Dept Life Sci, Modena, Italy Univ Modena & Reggio Emilia, Dept Life Sci, Modena, ItalyCattin, Eleonora论文数: 0 引用数: 0 h-index: 0机构: Univ Modena & Reggio Emilia, Dept Life Sci, Modena, Italy Univ Modena & Reggio Emilia, Dept Life Sci, Modena, ItalyFerrari, Tommaso论文数: 0 引用数: 0 h-index: 0机构: Univ Modena & Reggio Emilia, Dept Life Sci, Modena, Italy Univ Modena & Reggio Emilia, Dept Life Sci, Modena, ItalyPedrazzoli, Eleonora论文数: 0 引用数: 0 h-index: 0机构: Univ Modena & Reggio Emilia, Dept Life Sci, Modena, Italy Univ Modena & Reggio Emilia, Dept Life Sci, Modena, ItalyMarchionni, Matteo论文数: 0 引用数: 0 h-index: 0机构: Univ Modena & Reggio Emilia, Dept Life Sci, Modena, Italy Univ Modena & Reggio Emilia, Dept Life Sci, Modena, ItalyRossi, Rachele论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp S Anna Ferrara, Ferrara, Italy Univ Modena & Reggio Emilia, Dept Life Sci, Modena, ItalyD'Amico, Adele论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Childrens Res Hosp IRCCS, Unit Neuromuscular & Neurodegenerat Disorders, Dept Neurosci, Rome, Italy Univ Modena & Reggio Emilia, Dept Life Sci, Modena, ItalyMerlini, Luciano论文数: 0 引用数: 0 h-index: 0机构: Univ Bologna, Dept Biomed & Neuromotor Sci, Bologna, Italy Univ Modena & Reggio Emilia, Dept Life Sci, Modena, ItalySabatelli, Patrizia论文数: 0 引用数: 0 h-index: 0机构: Bologna CNR, Mol Genet Inst, Bologna, Italy Univ Modena & Reggio Emilia, Dept Life Sci, Modena, ItalyFerlini, Alessandra论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp S Anna Ferrara, Ferrara, Italy Univ Modena & Reggio Emilia, Dept Life Sci, Modena, ItalyGualandi, Francesca论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp S Anna Ferrara, Ferrara, Italy Univ Modena & Reggio Emilia, Dept Life Sci, Modena, ItalyRecchia, Alessandra论文数: 0 引用数: 0 h-index: 0机构: Univ Modena & Reggio Emilia, Dept Life Sci, Modena, Italy Univ Modena & Reggio Emilia, Dept Life Sci, Modena, Italy
- [24] Novel COL6A3 frameshift variant in American Staffordshire Terrier dogs with Ullrich-like congenital muscular dystrophyJOURNAL OF VETERINARY INTERNAL MEDICINE, 2023, 37 (06) : 2504 - 2509Jankelunas, Leanne论文数: 0 引用数: 0 h-index: 0机构: Washington State Univ, Coll Vet Med, Dept Vet Clin Sci, Pullman, WA USA Washington State Univ, Coll Vet Med, Dept Vet Clin Sci, Pullman, WA USAMurthy, Vishal D.论文数: 0 引用数: 0 h-index: 0机构: Washington State Univ, Coll Vet Med, Dept Vet Clin Sci, Pullman, WA USA Washington State Univ, Coll Vet Med, Dept Vet Clin Sci, Bustad Hall, Pullman, WA 99164 USA Washington State Univ, Coll Vet Med, Dept Vet Clin Sci, Pullman, WA USAChen, Annie V.论文数: 0 引用数: 0 h-index: 0机构: Washington State Univ, Coll Vet Med, Dept Vet Clin Sci, Pullman, WA USA Washington State Univ, Coll Vet Med, Dept Vet Clin Sci, Pullman, WA USAMinor, Katie M.论文数: 0 引用数: 0 h-index: 0机构: Univ Minnesota, Coll Vet Med, Dept Vet Clin Sci, St Paul, MN USA Washington State Univ, Coll Vet Med, Dept Vet Clin Sci, Pullman, WA USAFriedenberg, Steven G.论文数: 0 引用数: 0 h-index: 0机构: Univ Minnesota, Coll Vet Med, Dept Vet Clin Sci, St Paul, MN USA Washington State Univ, Coll Vet Med, Dept Vet Clin Sci, Pullman, WA USACullen, Jonah N.论文数: 0 引用数: 0 h-index: 0机构: Univ Minnesota, Coll Vet Med, Dept Vet Clin Sci, St Paul, MN USA Washington State Univ, Coll Vet Med, Dept Vet Clin Sci, Pullman, WA USAGuo, Ling T.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif San Diego, Sch Med, Dept Pathol, La Jolla, CA USA Washington State Univ, Coll Vet Med, Dept Vet Clin Sci, Pullman, WA USAMickelson, James R.论文数: 0 引用数: 0 h-index: 0机构: Univ Minnesota, Coll Vet Med, Dept Vet & Biomed Sci, St Paul, MN USA Washington State Univ, Coll Vet Med, Dept Vet Clin Sci, Pullman, WA USAShelton, G. Diane论文数: 0 引用数: 0 h-index: 0机构: Univ Calif San Diego, Sch Med, Dept Pathol, La Jolla, CA USA Washington State Univ, Coll Vet Med, Dept Vet Clin Sci, Pullman, WA USA
- [25] A common COL6A1 deep-intronic pseudo-exon inserting mutation causes a distinct phenotype of Ullrich congenital muscular dystrophyNEUROMUSCULAR DISORDERS, 2017, 27 : S106 - S106Foley, A. Reghan论文数: 0 引用数: 0 h-index: 0机构: NINDS, NIH, Bldg 36,Rm 4D04, Bethesda, MD 20892 USA NINDS, NIH, Bldg 36,Rm 4D04, Bethesda, MD 20892 USADonkervoort, S.论文数: 0 引用数: 0 h-index: 0机构: NINDS, NIH, Bldg 36,Rm 4D04, Bethesda, MD 20892 USA NINDS, NIH, Bldg 36,Rm 4D04, Bethesda, MD 20892 USABolduc, V.论文数: 0 引用数: 0 h-index: 0机构: NINDS, NIH, Bldg 36,Rm 4D04, Bethesda, MD 20892 USA NINDS, NIH, Bldg 36,Rm 4D04, Bethesda, MD 20892 USAHu, Y.论文数: 0 引用数: 0 h-index: 0机构: NINDS, NIH, Bldg 36,Rm 4D04, Bethesda, MD 20892 USA NINDS, NIH, Bldg 36,Rm 4D04, Bethesda, MD 20892 USACummings, B.论文数: 0 引用数: 0 h-index: 0机构: Harvard Med Sch, Broad Inst, Massachusetts Gen Hosp, Analyt & Translat Genet Unit, Cambridge, MA USA NINDS, NIH, Bldg 36,Rm 4D04, Bethesda, MD 20892 USALek, M.论文数: 0 引用数: 0 h-index: 0机构: Harvard Med Sch, Broad Inst, Massachusetts Gen Hosp, Analyt & Translat Genet Unit, Cambridge, MA USA NINDS, NIH, Bldg 36,Rm 4D04, Bethesda, MD 20892 USASarkozy, A.论文数: 0 引用数: 0 h-index: 0机构: UCL Inst Child Hlth, Dubowitz Neuromuscular Ctr, London, England NINDS, NIH, Bldg 36,Rm 4D04, Bethesda, MD 20892 USAJimenez-Mallebrera, C.论文数: 0 引用数: 0 h-index: 0机构: Hosp St Joan de Deu, Neuropediat Dept, Neuromuscular Unit, Barcelona, Spain NINDS, NIH, Bldg 36,Rm 4D04, Bethesda, MD 20892 USA论文数: 引用数: h-index:机构:Lamande, S.论文数: 0 引用数: 0 h-index: 0机构: Murdoch Childrens Res Inst, Parkville, Vic, Australia NINDS, NIH, Bldg 36,Rm 4D04, Bethesda, MD 20892 USAKirschner, J.论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr, Div Neuropediat & Muscle Disorders, Freiburg, Germany NINDS, NIH, Bldg 36,Rm 4D04, Bethesda, MD 20892 USAAllamand, V.论文数: 0 引用数: 0 h-index: 0机构: UPMC, Inserm UMRS974, Inst Myol, Ctr Res Myol,CNRS FRE3617, Paris, France NINDS, NIH, Bldg 36,Rm 4D04, Bethesda, MD 20892 USAStojkovic, T.论文数: 0 引用数: 0 h-index: 0机构: Inst Myol, Paris, France Grp Hosp Pitie Salpetriere, AP HP, Ctr Reference Malad Neuromusculaires, Paris, France NINDS, NIH, Bldg 36,Rm 4D04, Bethesda, MD 20892 USAQuijano-Roy, S.论文数: 0 引用数: 0 h-index: 0机构: Raymond Poincare Univ Hosp UVSQ, Garches Neuromuscular Ctr GNMH, Garches, France NINDS, NIH, Bldg 36,Rm 4D04, Bethesda, MD 20892 USA论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Bertini, E.论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Pediat Hosp, Unit Neuromuscular & Neurodegenerat Disorders, Lab Mol Med, IRCCS, Rome, Italy NINDS, NIH, Bldg 36,Rm 4D04, Bethesda, MD 20892 USAMacArthur, D.论文数: 0 引用数: 0 h-index: 0机构: Harvard Med Sch, Broad Inst, Massachusetts Gen Hosp, Analyt & Translat Genet Unit, Cambridge, MA USA NINDS, NIH, Bldg 36,Rm 4D04, Bethesda, MD 20892 USAMuntoni, F.论文数: 0 引用数: 0 h-index: 0机构: UCL Inst Child Hlth, Dubowitz Neuromuscular Ctr, London, England NINDS, NIH, Bldg 36,Rm 4D04, Bethesda, MD 20892 USABonnemann, C.论文数: 0 引用数: 0 h-index: 0机构: NINDS, NIH, Bldg 36,Rm 4D04, Bethesda, MD 20892 USA NINDS, NIH, Bldg 36,Rm 4D04, Bethesda, MD 20892 USA
- [26] Endoplasmic reticulum retention of COL6 chains in Ullrich congenital muscular dystrophyNEUROMUSCULAR DISORDERS, 2007, 17 (9-10) : 833 - 833Allamand, V.论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 06, Grp Hosp Pitie Salpetriere, INSERM, Inst Myol,U582,IFR14,RFDMC, Paris, France Univ Paris 06, Grp Hosp Pitie Salpetriere, INSERM, Inst Myol,U582,IFR14,RFDMC, Paris, FranceGartioux, C.论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 06, Grp Hosp Pitie Salpetriere, INSERM, Inst Myol,U582,IFR14,RFDMC, Paris, France Univ Paris 06, Grp Hosp Pitie Salpetriere, INSERM, Inst Myol,U582,IFR14,RFDMC, Paris, FranceLacene, E.论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 06, Grp Hosp Pitie Salpetriere, INSERM, Inst Myol,U582,IFR14, Paris, France Univ Paris 06, Grp Hosp Pitie Salpetriere, INSERM, Inst Myol,U582,IFR14,RFDMC, Paris, FranceLaine, J.论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 06, Grp Hosp Pitie Salpetriere, INSERM, Inst Myol,U582,IFR14, Paris, France Univ Paris 06, Grp Hosp Pitie Salpetriere, INSERM, Inst Myol,U582,IFR14,RFDMC, Paris, FranceLedeuil, C.论文数: 0 引用数: 0 h-index: 0机构: Grp Hosp Pitie Salpetriere, AP HP, UF Cardiogenet & Myogenet, Serv Biochim Metab, F-75634 Paris, France Univ Paris 06, Grp Hosp Pitie Salpetriere, INSERM, Inst Myol,U582,IFR14,RFDMC, Paris, FranceQuijano-Roy, S.论文数: 0 引用数: 0 h-index: 0机构: Hop Raymond Poincare, Francais Rech DMC, AP HP, Serv Pediat, Garches, France Univ Paris 06, Grp Hosp Pitie Salpetriere, INSERM, Inst Myol,U582,IFR14,RFDMC, Paris, FranceMakri, S.论文数: 0 引用数: 0 h-index: 0机构: Etablissement Hosp Specialise Ali Ait Idir, Algiers, Algeria Univ Paris 06, Grp Hosp Pitie Salpetriere, INSERM, Inst Myol,U582,IFR14,RFDMC, Paris, FranceViollet, L.论文数: 0 引用数: 0 h-index: 0机构: Hop Necker Enfants Malad, Francais Rech DMC, AP HP, Serv Genet, Paris, France Univ Paris 06, Grp Hosp Pitie Salpetriere, INSERM, Inst Myol,U582,IFR14,RFDMC, Paris, FranceJeannet, P.论文数: 0 引用数: 0 h-index: 0机构: CHUV, BH11, Unite Neuropediat, Lausanne, Switzerland Univ Paris 06, Grp Hosp Pitie Salpetriere, INSERM, Inst Myol,U582,IFR14,RFDMC, Paris, FranceHerlicoviez, D.论文数: 0 引用数: 0 h-index: 0机构: CHU Caen, F-14000 Caen, France Univ Paris 06, Grp Hosp Pitie Salpetriere, INSERM, Inst Myol,U582,IFR14,RFDMC, Paris, FrancePenniello-Valette, M.论文数: 0 引用数: 0 h-index: 0机构: CHU Caen, F-14000 Caen, France Univ Paris 06, Grp Hosp Pitie Salpetriere, INSERM, Inst Myol,U582,IFR14,RFDMC, Paris, FranceRichard, P.论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 06, Grp Hosp Pitie Salpetriere, INSERM,AP HP,U5882, Inst Myol,Serv Biochim Metab,UF Cardiogenet & Myo, Paris, France Univ Paris 06, Grp Hosp Pitie Salpetriere, INSERM, Inst Myol,U582,IFR14,RFDMC, Paris, FranceEstournet, B.论文数: 0 引用数: 0 h-index: 0机构: Hop Raymond Poincare, Francais Rech DMC, AP HP, Serv Pediat, Garches, France Univ Paris 06, Grp Hosp Pitie Salpetriere, INSERM, Inst Myol,U582,IFR14,RFDMC, Paris, FranceRomero, N.论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 06, Grp Hosp Pitie Salpetriere, INSERM, Inst Myol,U582,IFR14,RFDMC, Paris, France Univ Paris 06, Grp Hosp Pitie Salpetriere, INSERM, Inst Myol,U582,IFR14,RFDMC, Paris, FranceGuicheney, P.论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 06, Grp Hosp Pitie Salpetriere, INSERM, Inst Myol,U582,IFR14,RFDMC, Paris, France Univ Paris 06, Grp Hosp Pitie Salpetriere, INSERM, Inst Myol,U582,IFR14,RFDMC, Paris, France
- [27] CRISPR/Cas9 allele-specific design to inactivate a dominant-negative mutation in COL6A1 causing Ullrich muscular dystrophyHUMAN GENE THERAPY, 2021, 32 (19-20) : A65 - A66Benati, D.论文数: 0 引用数: 0 h-index: 0机构: Univ Modena & Reggio Emilia, Dept Life Sci, Modena, Italy Univ Modena & Reggio Emilia, Dept Life Sci, Modena, ItalyPatrizi, C.论文数: 0 引用数: 0 h-index: 0机构: Univ Modena & Reggio Emilia, Dept Life Sci, Modena, Italy Univ Modena & Reggio Emilia, Dept Life Sci, Modena, ItalyCattin, E.论文数: 0 引用数: 0 h-index: 0机构: Univ Modena & Reggio Emilia, Dept Life Sci, Modena, Italy Univ Modena & Reggio Emilia, Dept Life Sci, Modena, ItalyFerrari, T.论文数: 0 引用数: 0 h-index: 0机构: Univ Modena & Reggio Emilia, Dept Life Sci, Modena, Italy Univ Modena & Reggio Emilia, Dept Life Sci, Modena, ItalyPedrazzoli, E.论文数: 0 引用数: 0 h-index: 0机构: Univ Modena & Reggio Emilia, Dept Life Sci, Modena, Italy Univ Modena & Reggio Emilia, Dept Life Sci, Modena, ItalyMarchionni, M.论文数: 0 引用数: 0 h-index: 0机构: Univ Modena & Reggio Emilia, Dept Life Sci, Modena, Italy Univ Modena & Reggio Emilia, Dept Life Sci, Modena, ItalyRossi, R.论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp S Anna Ferrara, Ferrara, Italy Univ Modena & Reggio Emilia, Dept Life Sci, Modena, ItalyD'Amico, A.论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Childrens Res Hosp IRCCS, Dept Neurosci, Unit Neuromuscular & Neurodegenerat Disorders, Rome, Italy Univ Modena & Reggio Emilia, Dept Life Sci, Modena, ItalyMerlini, L.论文数: 0 引用数: 0 h-index: 0机构: Univ Bologna, Dept Biomed & Neuromotor Sci, Bologna, Italy Univ Modena & Reggio Emilia, Dept Life Sci, Modena, ItalySabatelli, P.论文数: 0 引用数: 0 h-index: 0机构: Bologna CNR, Mol Genet Inst, Bologna, Italy Univ Modena & Reggio Emilia, Dept Life Sci, Modena, ItalyFerlini, A.论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp S Anna Ferrara, Ferrara, Italy Univ Modena & Reggio Emilia, Dept Life Sci, Modena, ItalyGualandi, F.论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp S Anna Ferrara, Ferrara, Italy Univ Modena & Reggio Emilia, Dept Life Sci, Modena, ItalyRecchia, A.论文数: 0 引用数: 0 h-index: 0机构: Univ Modena & Reggio Emilia, Dept Life Sci, Modena, Italy Univ Modena & Reggio Emilia, Dept Life Sci, Modena, Italy
- [28] Generation of a human induced pluripotent stem cell line (CRICKi021-A) from a patient with Ullrich congenital muscular dystrophy carrying a pathogenic mutation in the COL6A1 geneSTEM CELL RESEARCH, 2025, 83Jiang, Yunsong论文数: 0 引用数: 0 h-index: 0机构: UCL, Dept Cell & Dev Biol, London WC1E 6DE, England Francis Crick Inst, Stem Cells & Neuromuscular Regenerat Lab, 1 Midland Rd, London NW1 1AT, England UCL, Dept Cell & Dev Biol, London WC1E 6DE, EnglandDevito, Liani G.论文数: 0 引用数: 0 h-index: 0机构: Francis Crick Inst, Human Embryo & Stem Cell Unit, London, England UCL, Dept Cell & Dev Biol, London WC1E 6DE, EnglandMuntoni, Francesco论文数: 0 引用数: 0 h-index: 0机构: UCL Great Ormond St Inst Child Hlth, Dubowitz Neuromuscular Ctr, London, England Great Ormond St Hosp Sick Children, London, England UCL, Dept Cell & Dev Biol, London WC1E 6DE, England论文数: 引用数: h-index:机构:Tedesco, Francesco Saverio论文数: 0 引用数: 0 h-index: 0机构: UCL, Dept Cell & Dev Biol, London WC1E 6DE, England Francis Crick Inst, Stem Cells & Neuromuscular Regenerat Lab, 1 Midland Rd, London NW1 1AT, England UCL Great Ormond St Inst Child Hlth, Dubowitz Neuromuscular Ctr, London, England Great Ormond St Hosp Sick Children, London, England UCL, Dept Cell & Dev Biol, London WC1E 6DE, England
- [29] 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
- [30] A rare case report: Bethlem myopathy and ullrich congenital muscular dystrophyJOURNAL OF THE NEUROLOGICAL SCIENCES, 2017, 381 : 272 - 272Tamura, P. R.论文数: 0 引用数: 0 h-index: 0机构: Univ City Sao Paulo, Neurol, Sao Paulo, Brazil Univ City Sao Paulo, Neurol, Sao Paulo, BrazilLegoroff, R.论文数: 0 引用数: 0 h-index: 0机构: Univ City Sao Paulo, Neurol, Sao Paulo, Brazil Univ City Sao Paulo, Neurol, Sao Paulo, BrazilCrotti, L. P.论文数: 0 引用数: 0 h-index: 0机构: Univ City Sao Paulo, Neurol, Sao Paulo, Brazil Univ City Sao Paulo, Neurol, Sao Paulo, BrazilGodoy, A. J.论文数: 0 引用数: 0 h-index: 0机构: Univ City Sao Paulo, Neurol, Sao Paulo, Brazil Univ City Sao Paulo, Neurol, Sao Paulo, Brazil