Referenced in: none

Automatically associated channels: Kir2.3 , Kv11.1

Title: Clinical, genetic, and biophysical characterization of a homozygous HERG mutation causing severe neonatal long QT syndrome.

Authors: Walter H Johnson, Ping Yang, Tao Yang, Yung R Lau, Barbara A Mostella, Daynna J Wolff, Dan M Roden, D Woodrow Benson

Journal, date & volume: Pediatr. Res., 2003 May , 53, 744-8

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/12621127

Abstract