Functional dominant-negative mutation of sodium channel subunit gene SCN3B associated with atrial fibrillation in a Chinese GeneID population

Atrial fibrillation (AF) is the most common cardiac arrhythmia in the clinic, and accounts for more than 15% of strokes. Mutations in cardiac sodium channel α, β1 and β2 subunit genes (SCN5A, SCN1B, and SCN2B) have been identified in AF patients. We hypothesize that mutations in the sodium channel β...

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Detalhes bibliográficos
Main Authors: Wang, Pengyun, Yang, Qinbo, Wu, Xiaofen, Yang, Yanzong, Shi, Lisong, Wang, Chuchu, Wu, Gang, Xia, Yunlong, Yang, Bo, Zhang, Rongfeng, Xu, Chengqi, Cheng, Xiang, Li, Sisi, Zhao, Yuanyuan, Fu, Fenfen, Liao, Yuhua, Fang, Fang, Chen, Qiuyun, Tu, Xin, Wang, Qing K.
Formato: Artigo
Idioma:Inglês
Publicado em: 2010
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3132081/
https://ncbi.nlm.nih.gov/pubmed/20558140
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bbrc.2010.06.042
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