Young and early‐onset dilated cardiomyopathy with malignant ventricular arrhythmia and sudden cardiac death induced by the heterozygous LDB3, MYH6, and SYNE1 missense mutations

BACKGROUND: The whole exome sequencing (WES) with targeted gene analysis is an effective diagnostic tool for cardiomyopathy. The early‐onset sudden cardiac death (SCD) was commonly associated with dilated cardiomyopathy (DCM) induced by pathogenic genetic mutations. METHODS: In a Chinese Han family,...

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Detalhes bibliográficos
Publicado no:Ann Noninvasive Electrocardiol
Main Authors: Zhao, Ting, Ma, Yuting, Zhang, Zuoquan, Xian, Jianzhong, Geng, Xiaojing, Wang, Feng, Huang, Jiana, Yang, Zhe, Luo, Yi, Lin, Yubi
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2021
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8293610/
https://ncbi.nlm.nih.gov/pubmed/33949037
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/anec.12840
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