We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleKv1.5 channelopathy due to KCNA5 loss-of-function mutation causes human atrial fibrillation.AuthorsOlson TM; Alekseev AE; Liu XK; Park S; Zingman LV; Bienengraeber M; Sattiraju S; Ballew JD; Jahangir A; Terzic APublicationHuman molecular genetics, 2006, Vol 15, Issue 14, p2185ISSN0964-6906Publication typearticleDOI10.1093/hmg/ddl143