Diagnostic criteria for the limb-girdle muscular dystrophies: Report of the ENMC consortium on limbgirdle dystrophies
- 31 January 1995
- journal article
- research article
- Published by Elsevier in Neuromuscular Disorders
- Vol. 5 (1), 71-74
- https://doi.org/10.1016/0960-8966(93)e0006-g
Abstract
No abstract availableThis publication has 17 references indexed in Scilit:
- Linkage of Tunisian autosomal recessive Duchenne–like muscular dystrophy to the pericentromeric region of chromosome 13qNature Genetics, 1992
- Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophyNature, 1992
- Confirmation of linkage of limb-girdle muscular dystrophy, type 2, to chromosome 15Genomics, 1992
- Benign muscular dystrophy with autosomal dominant inheritanceNeuromuscular Disorders, 1991
- Limb girdle muscular dystrophy with autosomal dominant inheritanceActa Neurologica Scandinavica, 1991
- Adult‐onset autosomal dominant limb‐girdle muscular dystrophyAnnals of Neurology, 1986
- Severe childhood muscular dystrophy affecting both sexes and frequent in tunisiaMuscle & Nerve, 1983
- BENIGN MYOPATHY, WITH AUTOSOMAL DOMINANT INHERITANCEBrain, 1976
- A Late Autosomal Dominant Form of Limb-Girdle Muscular DystrophyEuropean Neurology, 1974
- ON THE CLASSIFICATION, NATURAL HISTORY AND TREATMENT OF THE MYOPATHIESBrain, 1954