Citations for
1ATFB7, KCNA5
Novel KCNA5 mutation implicates tyrosine kinase signaling in human atrial fibrillation.
Yang T, Yang P, Roden DM, Darbar D.
Heart Rhythm 7(9):1246-52. doi: 10.1016/j.hrthm.2010.05.032. Epub 2010 Jun 1. 2010
2ATFB7, KCNA5
Kv1.5 channelopathy due to KCNA5 loss-of-function mutation causes human atrial fibrillation.
Olson TM, Alekseev AE, Liu XK, Park S, Zingman LV, Bienengraeber M, Sattiraju S, Ballew JD, Jahangir A, Terzic A.
Hum Mol Genet 15(14):2185-91. Epub 2006 Jun 13. 2006