Referenced in: none

Automatically associated channels: Kv12.1 , Nav1.5 , Slo1

Title: A heterozygous deletion mutation in the cardiac sodium channel gene SCN5A with loss- and gain-of-function characteristics manifests as isolated conduction disease, without signs of Brugada or long QT syndrome.

Authors: Sven Zumhagen, Marieke W Veldkamp, Birgit Stallmeyer, Antonius Baartscheer, Lars Eckardt, Matthias Paul, Carol Ann Remme, Zahurul A Bhuiyan, Connie R Bezzina, Eric Schulze-Bahr

Journal, date & volume: PLoS ONE, 2013 , 8, e67963

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/23840796

Abstract