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Updated: May 30, 2025

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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[Hypertrophic obstructive cardiomyopathy associated with Fabry disease: a case report]

Y K Liu1, Q P Shi2, X Y Luo1

  • 1Department of Cardiology, Peking University First Hospital, Beijing100034, China.

Zhonghua Nei Ke Za Zhi
|January 25, 2025
PubMed
Summary

No abstract available in PubMed .

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