関連する実験動画

Updated: Jun 15, 2026

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

DNAシーケンシングによる重度の因子VII欠乏症の産前排除

D S Millar, D N Cooper, V V Kakkar

    Lancet (London, England)
    |May 30, 1992
    PubMed
    まとめ

    No abstract available in PubMed .

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