Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity
- 1 June 1995
- journal article
- letter
- Published by Springer Science and Business Media LLC in Nature Genetics
- Vol. 10 (2), 243-245
- https://doi.org/10.1038/ng0695-243
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Adhalin gene polymorphismHuman Molecular Genetics, 1994
- Selective Defect of Sarcoglycan Complex in Severe Childhood Autosomal Recessive Muscular Dystrophy MuscleBiochemical and Biophysical Research Communications, 1994
- Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophyCell, 1994
- Linkage analysis of families with severe childhood autosomal recessive muscular dystrophy in Morocco indicates genetic homogeneity of the disease in north Africa.Journal of Medical Genetics, 1994
- Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12Human Molecular Genetics, 1993
- 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
- Membrane organization of the dystrophin-glycoprotein complexCell, 1991
- Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscleNature, 1990
- Severe childhood muscular dystrophy affecting both sexes and frequent in tunisiaMuscle & Nerve, 1983