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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Detalles Bibliográficos
Autores principales: Zhao, Ting, Ma, Yuting, Zhang, Zuoquan, Xian, Jianzhong, Geng, Xiaojing, Wang, Feng, Huang, Jiana, Yang, Zhe, Luo, Yi, Lin, Yubi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8293610/
https://www.ncbi.nlm.nih.gov/pubmed/33949037
http://dx.doi.org/10.1111/anec.12840

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