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Updated: Jun 20, 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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[A pedigree with hypertrophic cardiomyopathy caused by a thyroxine translocator c.128G>A mutation]
1Department of Cardiology, Beijing Anzhen Hospital, Capital Medical University, Beijing Institute of Heart Lung & Blood Vessel Diseases, Beijing 100029, China.
Zhonghua Xin Xue Guan Bing Za Zhi
|July 17, 2024
Abstract
No abstract available in PubMed .
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