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Updated: May 12, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model

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Variations in the PDCD6 gene are associated with increased uterine leiomyoma risk in the Chinese

Kui Zhang1, Bin Zhou, Shaoqing Shi

  • 1Department of Forensic Biology, West China School of Preclinical and Forensic Medicine, Sichuan University, Chengdu, People's Republic of China.

Genetic Testing and Molecular Biomarkers
|April 5, 2013
PubMed

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