Genome-wide screening identifies a KCNIP1 copy number variant as a genetic predictor for atrial fibrillation

Atrial fibrillation (AF) is the most common sustained cardiac arrhythmia. Previous genome-wide association studies had identified single-nucleotide polymorphisms in several genomic regions to be associated with AF. In human genome, copy number variations (CNVs) are known to contribute to disease sus...

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Publicado no:Nat Commun
Main Authors: Tsai, Chia-Ti, Hsieh, Chia-Shan, Chang, Sheng-Nan, Chuang, Eric Y., Ueng, Kwo-Chang, Tsai, Chin-Feng, Lin, Tsung-Hsien, Wu, Cho-Kai, Lee, Jen-Kuang, Lin, Lian-Yu, Wang, Yi-Chih, Yu, Chih-Chieh, Lai, Ling-Ping, Tseng, Chuen-Den, Hwang, Juey-Jen, Chiang, Fu-Tien, Lin, Jiunn-Lee
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2016
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4740744/
https://ncbi.nlm.nih.gov/pubmed/26831368
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ncomms10190
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