Analysis of a Family with Brugada Syndrome and Sudden Cardiac Death Caused by a Novel Mutation of SCN5A

BACKGROUND: Brugada syndrome is a hereditary cardiac disease associated with mutations in ion channel genes. The clinical features include ventricular fibrillation, syncope, and sudden cardiac death. A family with Brugada syndrome with sudden cardiac death was analyzed to locate the associated mutat...

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Detalles Bibliográficos
Autores principales: Zhu, Yao-Bin, Zhang, Jian-Hui, Ji, Yuan-Yuan, Hu, Ya-Nan, Wang, Han-Lu, Ruan, Dan-Dan, Meng, Xiao-Rong, Lin, Xin-Fu, Luo, Jie-Wei, Chen, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072018/
https://www.ncbi.nlm.nih.gov/pubmed/35529058
http://dx.doi.org/10.1155/2022/9716045

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072018/
https://www.ncbi.nlm.nih.gov/pubmed/35529058
http://dx.doi.org/10.1155/2022/9716045

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