PubMed 10862094
Referenced in: none
Automatically associated channels: Kv11.1 , Kv7.1
Title: Survey of the coding region of the HERG gene in long QT syndrome reveals six novel mutations and an amino acid polymorphism with possible phenotypic effects.
Authors: P Laitinen, H Fodstad, K Piippo, H Swan, L Toivonen, M Viitasalo, J Kaprio, K Kontula
Journal, date & volume: Hum. Mutat., 2000 Jun , 15, 580-1
PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/10862094
Abstract