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Updated: Jul 29, 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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METTL1 gene polymorphisms and Wilms tumor susceptibility in Chinese children: A five-center case-control study
Linqing Deng1, Ruixi Hua1, Zhengtao Zhang1
1Department of Pediatric Surgery, Guangzhou Institute of Pediatrics, Guangdong Provincial Key Laboratory of Research in Structural Birth Defect Disease, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, Guangdong 510623, China.
Chinese Medical Journal
|May 26, 2023
Abstract
No abstract available in PubMed .
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