High prevalence of genetic variants previously associated with LQT syndrome in new exome dataREFSGAARD, Lena; HOLST, Anders G; SADJADIEH, Golnaz et al.European journal of human genetics. 2012, Vol 20, Num 8, pp 905-908, issn 1018-4813, 4 p.Article

Familial Aggregation of Lone Atrial Fibrillation in Young PersonsØYEN, Nina; RANTHE, Mattis F; CARSTENSEN, Lisbeth et al.Journal of the American College of Cardiology. 2012, Vol 60, Num 10, pp 917-921, issn 0735-1097, 5 p.Article

Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillationOLESEN, Morten S; JESPERSEN, Thomas; SCHMITT, Nicole et al.Cardiovascular research. 2011, Vol 89, Num 4, pp 786-793, issn 0008-6363, 8 p.Article