We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleMolecular genetic analysis of long QT syndrome in Norway indicating a high prevalence of heterozygous mutation carriers.AuthorsBerge KE; Haugaa KH; Früh A; Anfinsen OG; Gjesdal K; Siem G; Oyen N; Greve G; Carlsson A; Rognum TO; Hallerud M; Kongsgård E; Amlie JP; Leren TPPublicationScandinavian journal of clinical and laboratory investigation, 2008, Vol 68, Issue 5, p362ISSN0036-5513Publication typearticleDOI10.1080/00365510701765643