A novel KCND3 mutation associated with early-onset lone atrial fibrillation

Atrial fibrillation (AF) is the most common arrhythmia in the clinic. While previous studies have identified AF-associated mutations in several genes, the genetic basis for AF remains unclear. Here, we identified a novel T361S missense mutation in potassium voltage-gated channel, shal-related subfam...

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Detalles Bibliográficos
Autores principales: Huang, Yuan, Yang, Jiawei, Xie, Wanyi, Li, Qince, Zeng, Zhipeng, Sui, Haibo, Shan, Zhonggui, Huang, Zhengrong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5777789/
https://www.ncbi.nlm.nih.gov/pubmed/29383177
http://dx.doi.org/10.18632/oncotarget.23303

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5777789/
https://www.ncbi.nlm.nih.gov/pubmed/29383177
http://dx.doi.org/10.18632/oncotarget.23303

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