Limb-Girdle Muscular Dystrophy in the United States
Open Access
- 1 October 2006
- journal article
- research article
- Published by Oxford University Press (OUP) in Journal of Neuropathology and Experimental Neurology
- Vol. 65 (10) , 995-1003
- https://doi.org/10.1097/01.jnen.0000235854.77716.6c
Abstract
Limb-girdle muscular dystrophy (LGMD) has been linked to 15 chromosomal loci, 7 autosomal-dominant (LGMD1A to E) and 10 autosomal-recessive (LGMD2A tKeywords
This publication has 75 references indexed in Scilit:
- Systemic delivery of morpholino oligonucleotide restores dystrophin expression bodywide and improves dystrophic pathologyNature Medicine, 2006
- Dystroglycan: from biosynthesis to pathogenesis of human diseaseJournal of Cell Science, 2006
- Calpain-3 mutations in TurkeyEuropean Journal of Pediatrics, 2006
- Extension of the clinical range of facioscapulohumeral dystrophy: report of six casesJournal of Neurology, Neurosurgery & Psychiatry, 2000
- A cross section of autosomal recessive limb-girdle muscular dystrophies in 38 familiesJournal of Medical Genetics, 2000
- Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethoninNature Genetics, 2000
- Rescue of Skeletal Muscles of γ-Sarcoglycan- Deficient Mice with Adeno-Associated Virus-Mediated Gene TransferMolecular Therapy, 2000
- Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2ACell, 1995
- Population frequencies of inherited neuromuscular diseases—A world surveyNeuromuscular Disorders, 1991
- ON THE CLASSIFICATION, NATURAL HISTORY AND TREATMENT OF THE MYOPATHIESBrain, 1954