Related Experiment Video
Updated: Jul 6, 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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[Clinical characteristics and gene mutation analysis of two families with hereditary protein C deficiency]
M L Zeng1, L L Yang1, A Q Zou1
1Department of Clinical Laboratory, the First Affiliated Hospital of Wenzhou Medical University, Key Laboratory of Clinical Laboratory Diagnosis and Translational Research of Zhejiang Province, Wenzhou 325015, China.
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi
|January 7, 2024
Abstract
No abstract available in PubMed .
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