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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

[Gene (SCN5A) mutation analysis of a Chinese family with Brugada syndrome]

Li Tian1, Jian-Fang Zhu, Jun-Guo Yang

  • 1Institute of Cardiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.

Zhonghua Xin Xue Guan Bing Za Zhi
|March 18, 2008
PubMed
Abstract

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