Referenced in: none

Automatically associated channels: Kv7.1

Title: A novel mutation in KVLQT1, L122P, found in a family with autosomal dominant long QT syndrome.

Authors: A D Krahn, J Wang, B Spindler, A C Skanes, R Yee, G J Klein, R A Hegele

Journal, date & volume: Am. Heart J., 2000 Jul , 140, 146-9

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/10874277

Abstract