Referenced in: none

Automatically associated channels: Kv11.1 , Kv7.1 , Nav1.5

Title: Molecular genetic analysis of long QT syndrome in Norway indicating a high prevalence of heterozygous mutation carriers.

Authors: K E Berge, K H Haugaa, A Früh, O-G Anfinsen, K Gjesdal, G Siem, N Oyen, G Greve, A Carlsson, T O Rognum, M Hallerud, E Kongsgård, J P Amlie, T P Leren

Journal, date & volume: Scand. J. Clin. Lab. Invest., 2008 , 68, 362-8

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/18752142

Abstract