Referenced in: none

Automatically associated channels: Kv7.1

Title: Heterozygous mutation in the pore of potassium channel gene KvLQT1 causes an apparently normal phenotype in long QT syndrome.

Authors: N Neyroud, I Denjoy, C Donger, F Gary, E Villain, A Leenhardt, K Benali, K Schwartz, P Coumel, P Guicheney

Journal, date & volume: Eur. J. Hum. Genet., 1998 Mar-Apr , 6, 129-33

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/9781056

Abstract