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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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[A case of type 2A juvenile hereditary hemochromatosis]

J L Fan1, B Y Zhou1, Y L Dai1

  • 1Department of Cardiology, the First Affiliated Hospital of Soochow University, Suzhou215031, China.

Zhonghua Xin Xue Guan Bing Za Zhi
|January 14, 2025
PubMed
Abstract

No abstract available in PubMed .

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