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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...
Autores principales: | Huang, Yuan, Yang, Jiawei, Xie, Wanyi, Li, Qince, Zeng, Zhipeng, Sui, Haibo, Shan, Zhonggui, Huang, Zhengrong |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
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 |
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