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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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Genetics: Titin mutation segregates with hereditary myopathy with respiratory failure

Iley Ozerlat

    Nature Reviews. Neurology
    |June 13, 2012
    PubMed
    Abstract

    No abstract available in PubMed .

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