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Updated: Feb 11, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
Identification of a novel missense KRT86 mutation in a Chinese family with monilethrix
Ying Deng1,2,3, Dengmei Xia4, Lian Wang5
1National Office for Maternal and Child Health Surveillance of China, Department of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, China.
No abstract available in PubMed .
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