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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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A large GLC1C Greek family with a myocilin T377M mutation: inheritance and phenotypic variability

Michael B Petersen1, George Kitsos, John R Samples

  • 1Department of Genetics, Institute of Child Health, Athens, Greece.

Investigative Ophthalmology & Visual Science
|January 25, 2006
PubMed
Abstract

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