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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model

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The p.G154S mutation of the alpha-B crystallin gene (CRYAB) causes late-onset distal myopathy

Peter Reilich1, Benedikt Schoser, Nicolai Schramm

  • 1Friedrich-Baur-Institute, Department of Neurology, University of Munich, D-80336 Munich, Germany. eilich@lrz.uni-muenchen.de

Neuromuscular Disorders : NMD
|February 23, 2010
PubMed

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