Identification of rare heterozygous linkage R965C‐R1309H mutations in the pore‐forming region of SCN5A gene associated with complex arrhythmia

BACKGROUND: We examined the genetic background of a Chinese Han family in which some members presented with complex arrhythmias including sick sinus syndrome, progressive conduction block, atrial fibrillation, atrial standstill and Brugada syndrome. The possible underlying mechanism associated with...

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Detalles Bibliográficos
Autores principales: Lin, Yubi, Qin, Jiading, Shen, Yuhui, Huang, Jiana, Zhang, Zuoquan, Zhu, ZhiLing, Lu, Huifang, Huang, Yin, Yin, Yuelan, Wang, Ani, Jin, Lizi, Hu, Zhenyu, Lin, Xiufang, Jiang, Bin
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/PMC8172209/
https://www.ncbi.nlm.nih.gov/pubmed/33764691
http://dx.doi.org/10.1002/mgg3.1613

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