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Disruption of the β-Sarcoglycan Gene Reveals Pathogenetic Complexity of Limb-Girdle Muscular Dystrophy Type 2E

  • Published:2000-01 Issue:1 Volume:5 Page:141-151
  • ISSN:1097-2765
  • Container-title:Molecular Cell
  • language:en
  • Short-container-title:Molecular Cell

Author:

Durbeej Madeleine,Cohn Ronald D.,Hrstka Ronald F.,Moore Steven A.,Allamand Valérie,Davidson Beverly L.,Williamson Roger A.,Campbell Kevin P.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology

Reference45 articles.

1. Mild congenital muscular dystrophy in two patients with an internally deleted laminin alpha2-chain;Allamand;Hum. Mol. Gen,1997

2. Loss of the sarcoglycan complex and sarcospan leads to muscular dystrophy in beta-sarcoglycan deficient mice;Araishi;Hum. Mol. Gen,1999

3. Gastric hypomotility in Duchenne's muscular dystrophy;Bahron;N. Engl. J. Med,1988

4. Disruption of heart sarcoglycan complex and severe cardiomyopathy caused by β-sarcoglycan mutations;Barresi;J. Med. Gen,1999

5. Beta-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex;Bönnemann;Nat. Genet,1995
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