PubMed 10790218
Referenced in: none
Automatically associated channels: Kv11.1 , Kv7.1
Title: Analysis of the human KCNH2(HERG) gene: identification and characterization of a novel mutation Y667X associated with long QT syndrome and a non-pathological 9 bp insertion.
Authors: A Paulussen, P Yang, M Pangalos, P Verhasselt, R Marrannes, C Verfaille, I Vandenberk, R Crabbe, F Konings, W Luyten, M Armstrong
Journal, date & volume: Hum. Mutat., 2000 May , 15, 483
PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/10790218
Abstract