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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
03:45

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

Published on: August 8, 2022

Human "nuclear" mitochondrial cardiomyopathy a novel mouse model characterizes the disease

Eloisa Arbustini, Maurizia Grasso

    JACC. Cardiovascular Imaging
    |January 15, 2011
    PubMed
    Abstract

    No abstract available in PubMed .

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