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Updated: Aug 6, 2026

03:45
Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
New compound heterozygous mutations in a Chinese family with lipoid proteinosis
C Y Wang1, P Z Zhang, F R Zhang
1Shandong Provincial Institute of Dermatology and Venereology, 57 Jiyan Road, Jinan, China.
The British Journal of Dermatology
|August 3, 2006
Abstract
No abstract available in PubMed .
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