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Desmin-related myopathy

Published:2010-07-21 Issue:4 Volume:80 Page:354-366
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

van Spaendonck-Zwarts KY,van Hessem L,Jongbloed JDH,de Walle HEK,Capetanaki Y,van der Kooi AJ,van Langen IM,van den Berg MP,van Tintelen JP

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2010.01512.x/fullpdf

Reference81 articles.

1. Myofibrillar myopathies.;Selcen;Curr Opin Neurol,2008

2. Desmin myopathy, a skeletal myopathy with cardiomyopathy caused by mutations in the desmin gene.;Dalakas;N Engl J Med,2000

3. Missense mutations in desmin associated with familial cardiac and skeletal myopathy.;Goldfarb;Nat Genet,1998

4. A missense mutation in the alphaB-crystallin chaperone gene causes a desmin-related myopathy.;Vicart;Nat Genet,1998

5. Myofibrillar myopathy caused by novel dominant negative alpha B-crystallin mutations.;Selcen;Ann Neurol,2003

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