PubMed 21483829
Referenced in: none
Automatically associated channels: Kv11.1 , Kv7.1 , Kv8.2
Title: Trafficking defect and proteasomal degradation contribute to the phenotype of a novel KCNH2 long QT syndrome mutation.
Authors: Anton Mihic, Vijay S Chauhan, Xiaodong Gao, Gavin Y Oudit, Robert G Tsushima
Journal, date & volume: PLoS ONE, 2011 , 6, e18273
PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/21483829
Abstract