Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Atrial Fibrillation and KCNE3[original query] |
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KCNQ1 gain-of-function mutation in familial atrial fibrillation. Science (New York, N.Y.) 2003 1 299 (5604): 251-4. Chen Yi-Han, Xu Shi-Jie, Bendahhou Said, Wang Xiao-Liang, Wang Ying, Xu Wen-Yuan, Jin Hong-Wei, Sun Hao, Su Xiao-Yan, Zhuang Qi-Nan, Yang Yi-Qing, Li Yue-Bin, Liu Yi, Xu Hong-Ju, Li Xiao-Fei, Ma Ning, Mou Chun-Ping, Chen Zhu, Barhanin Jacques, Huang W |
The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study. Journal of negative results in biomedicine 2011 10 (1): 12. Hedley Paula L, Haundrup Ole, Andersen Paal S, Aidt Frederik H, Jensen Morten, Moolman-Smook Johanna C, Bundgaard Henning, Christiansen Micha |
Gain-of-function mutations in potassium channel subunit KCNE2 associated with early-onset lone atrial fibrillation. Biomarkers in medicine 2014 8 (4): 557-70. Nielsen Jonas Bille, Bentzen Bo Hjorth, Olesen Morten Salling, David Jens-Peter, Olesen Søren-Peter, Haunsø Stig, Svendsen Jesper Hastrup, Schmitt Nico |
[Association study between the KCNE family gene polymorphisms of potassium channel gene and the susceptibility of atrial fibrillation]. Zhonghua yi xue za zhi 2022 Oct 102 (38): 3026-3032. Qin M, Tao J R, Liu Z J, Hu W Y, Yan P Y, Wang R, Zhang Y, Xu G |
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- Page last updated:Apr 29, 2024
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