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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Identification and molecular characterization of 18 novel mutations in the ATP7B gene from Indian Wilson disease

S Kumar, B R Thapa, G Kaur

    Clinical Genetics
    |April 7, 2005
    PubMed
    Abstract

    No abstract available in PubMed .

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