Channelpedia

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