Referenced in: none

Automatically associated channels: Kv7.1 , Slo1

Title: Dominant-negative KvLQT1 mutations underlie the LQT1 form of long QT syndrome.

Authors: F Y Shalaby, P C Levesque, W P Yang, W A Little, M L Conder, T Jenkins-West, M A Blanar

Journal, date & volume: Circulation, 1997 Sep 16 , 96, 1733-6

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/9323054

Abstract