Referenced in: none

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

Title: Four potassium channel mutations account for 73% of the genetic spectrum underlying long-QT syndrome (LQTS) and provide evidence for a strong founder effect in Finland.

Authors: Heidi Fodstad, Heikki Swan, Päivi Laitinen, Kirsi Piippo, Kristian Paavonen, Matti Viitasalo, Lauri Toivonen, Kimmo Kontula

Journal, date & volume: Ann. Med., 2004 , 36 Suppl 1, 53-63

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/15176425

Abstract