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Updated: Jun 6, 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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SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population

Asako Aoki1, Kouichi Ozaki, Hiroshi Sato

  • 1Laboratory for Cardiovascular Disease, Center for Genomic Medicine, RIKEN, Yokohama, Japan.

Journal of Human Genetics
|November 26, 2010
PubMed

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