ε-Sarcoglycan Replaces α-Sarcoglycan in Smooth Muscle to Form a Unique Dystrophin-Glycoprotein Complex

This publication has 43 references indexed in Scilit:

• Functional Rescue of the Sarcoglycan Complex in the BIO 14.6 Hamster Using δ-Sarcoglycan Gene Transfer
  Molecular Cell, 1998
• β-Sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolate
  Neuromuscular Disorders, 1998
• Human ϵ‐sarcoglycan is highly related to α‐sarcoglycan (adhalin), the limb girdle muscular dystrophy 2D gene¹
  FEBS Letters, 1998
• Characterization of δ-Sarcoglycan, a Novel Component of the Oligomeric Sarcoglycan Complex Involved in Limb-Girdle Muscular Dystrophy
  Published by Elsevier ,1996
• β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12
  Nature Genetics, 1995
• β–sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex
  Nature Genetics, 1995
• Three muscular dystrophies: Loss of cytoskeleton-extracellular matrix linkage
  Cell, 1995
• Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix
  Nature, 1992
• Gastric Hypomotility in Duchenne's Muscular Dystrophy
  New England Journal of Medicine, 1988
• Microvascular spasm in the cardiomyopathic Syrian hamster: a preventable cause of focal myocardial necrosis.
  Circulation, 1982