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Updated: Feb 17, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
MYH7 Rare Variant in a Family With Double-Chambered Left Ventricle
Jing Wang1, Xin Zhang1, Xi Wang1
1From the Department of Medical Genetics and Developmental Biology, School of Basic Medical Sciences (J.W.) and Heart Center, Beijing Children's Hospital (X.Z., F.W.), Capital Medical University, China; Center for Genetics, National Research Institute for Family Planning, Beijing (X.W., B.W.); and School of Life Sciences, Zhengzhou University, China (C.W.).
No abstract available in PubMed .
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