Related Experiment Video
Updated: Aug 27, 2025

03:45
Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
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Haploinsufficiency of syncoilin leads to hypertrophic cardiomyopathy
Liang-Liang Fan1,2,3, Zhuang-Zhuang Yuan1,2,3, Zi-Jun Jiao2,3
1Clinical Center for Gene Diagnosis and Therapy, Department of Cardiovascular Surgery, The Second Xiangya Hospital of Central South University, Changsha, Hunan 410011, PR China.
Genes & Diseases
|September 26, 2022
Abstract
No abstract available in PubMed .
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