β–sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex
- 1 November 1995
- journal article
- case report
- Published by Springer Science and Business Media LLC in Nature Genetics
- Vol. 11 (3), 266-273
- https://doi.org/10.1038/ng1195-266
Abstract
No abstract availableKeywords
This publication has 41 references indexed in Scilit:
- 30th and 31st ENMC international workshops, Naarden, The Netherlands, Held 6–8 January 1995Neuromuscular Disorders, 1995
- 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
- The 1993–94 Généthon human genetic linkage mapNature Genetics, 1994
- Characterization of NIGMS Human/Rodent Somatic Cell Hybrid Mapping Panel 2 by PCRGenomics, 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
- Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrixNature, 1992
- Basic local alignment search toolJournal of Molecular Biology, 1990
- Deglycosylation of asparagine-linked glycans by peptide:N-glycosidase FBiochemistry, 1985