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Updated: Jun 15, 2026

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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La exclusión prenatal de la deficiencia severa del factor VII mediante la secuenciación del ADN

D S Millar, D N Cooper, V V Kakkar

    Lancet (London, England)
    |May 30, 1992
    PubMed
    Resumen

    No abstract available in PubMed .

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