Referenced in: none

Automatically associated channels: Kv11.1 , Kv7.1

Title: Molecular characterization of two founder mutations causing long QT syndrome and identification of compound heterozygous patients.

Authors: Heidi Fodstad, Saïd Bendahhou, Jean-Sébastien Rougier, Päivi J Laitinen-Forsblom, Jacques Barhanin, Hugues Abriel, Laurent Schild, Kimmo Kontula, Heikki Swan

Journal, date & volume: Ann. Med., 2006 , 38, 294-304

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/16754261

Abstract