Deficiency of dystrophin-associated proteins: A common mechanism leading to muscle cell necrosis in severe childhood muscular dystrophies
- 31 December 1993
- journal article
- review article
- Published by Elsevier in Neuromuscular Disorders
- Vol. 3 (2) , 109-118
- https://doi.org/10.1016/0960-8966(93)90002-2
Abstract
No abstract availableKeywords
This publication has 37 references indexed in Scilit:
- Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains of dystrophin.Journal of Clinical Investigation, 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
- Glycoprotein‐binding site of dystrophin is confined to the cysteine‐rich domain and the first half of the carboxy‐terminal domainFEBS Letters, 1992
- An intact cysteine-rich domain is required for dystrophin function.Journal of Clinical Investigation, 1992
- Expression of the N‐terminal domain of dystrophin in E. coli and demonstration of binding to F‐actinFEBS Letters, 1992
- Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrixNature, 1992
- Is the carboxyl‐terminus of dystrophin required for membrane association? A novel, severe case of duchenne muscular dystrophyAnnals of Neurology, 1991
- Mosaic Expression of Dystrophin in Symptomatic Carriers of Duchenne's Muscular DystrophyNew England Journal of Medicine, 1989
- Characterization of Dystrophin in Muscle-Biopsy Specimens from Patients with Duchenne's or Becker's Muscular DystrophyNew England Journal of Medicine, 1988