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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Familial cardiac valvulopathy due to filamin A mutation

Jonathan A Bernstein1, Daniel Bernstein, Ute Hehr

  • 1Division of Medical Genetics, Department of Pediatrics, Stanford University School of Medicine, Stanford, California 94305-5208, USA. jon.bernstein@stanford.edu

American Journal of Medical Genetics. Part A
|August 5, 2011
PubMed

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