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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Multiple cerebral cavernous malformations and a novel CCM3 germline deletion in a German family

Chi-un Choe, Florence Riant, Christian Gerloff

    Journal of Neurology
    |July 13, 2010
    PubMed
    Abstract

    No abstract available in PubMed .

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