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Updated: Sep 4, 2025

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
Yunqing Ren1, Jipeng Liu1, Dianyi Yao1
1Department of Dermatology, The Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou, Zhejiang 310052, China.
No abstract available in PubMed .
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