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Updated: Dec 13, 2025

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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Precision Medicine and Dilated Cardiomyopathy.

Xiang Li1, Wenyan Zhu2,3

  • 1Department of Cardiology, The First Affiliated Hospital of Chongqing Medical University, Chongqing Medical University, Chongqing, China. lzd9288@163.com.

Methods in Molecular Biology (Clifton, N.J.)
|July 26, 2020
PubMed
Summary

Dilated cardiomyopathy (DCM) treatment is shifting towards precision medicine for better patient outcomes. This approach focuses on prevention and individualized care, moving beyond traditional heart failure management.

Keywords:
Dilated cardiomyopathyGene mutationGenetic detectionPathogenic genePrecision medicine

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