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Updated: Jul 6, 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

Case-control study of the role of the Gitelman's syndrome gene in essential hypertension

Noriko Aoi1, Tomohiro Nakayama, Naoyuki Sato

  • 1Division of Molecular Diagnostics, Department of Advanced Medical Science, Nihon University School of Medicine, Tokyo, Japan.

Endocrine Journal
|March 26, 2008
PubMed
Abstract

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