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Updated: Dec 31, 2025

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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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[A pathogenic mutation in the COPA gene causes a family of COPA syndrome]
K Z Lin1, F F Zhang2, J H Xiao1
1Department of Pediatrics, First Affiliated Hospital of Xiamen University, Xiamen 361000, China.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics
|January 7, 2020
Abstract
No abstract available in PubMed .
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