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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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[Genetic background of heart failure: SNP association study for heart failure and the underlying diseases]

Kouichi Ozaki1

  • 1Laboratory for Cardiovascular Diseases, RIKEN Center for Genomic Medicine, Yokohama 230-0045, Japan. ozakik@src.riken.jp

Rinsho Byori. the Japanese Journal of Clinical Pathology
|May 16, 2013
PubMed

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