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16. 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; 2006 Jul; 15(14):2185-91. PubMed ID: 16772329 [TBL] [Abstract][Full Text] [Related]
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