Related Experiment Video

Updated: Jul 19, 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

Genome-wide association study to identify single-nucleotide polymorphisms conferring risk of myocardial infarction

Kouichi Ozaki1, Toshihiro Tanaka

  • 1RIKEN, SNP Research Center, Tokyo, Japan.

Methods in Molecular Medicine
|October 31, 2006
PubMed

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