Referenced in: none

Automatically associated channels: Kir2.1 , Kv11.1 , Kv7.1 , Nav1.5

Title: A novel mutation in the transmembrane nonpore region of the KCNH2 gene causes severe clinical manifestations of long QT syndrome.

Authors: Li Liu, Kenshi Hayashi, Tomoya Kaneda, Hidekazu Ino, Noboru Fujino, Katsuharu Uchiyama, Tetsuo Konno, Toyonobu Tsuda, Masa-aki Kawashiri, Kosei Ueda, Toshinori Higashikata, Wen Shuai, Sabina Kupershmidt, Haruhiro Higashida, Masakazu Yamagishi

Journal, date & volume: Heart Rhythm, 2013 Jan , 10, 61-7

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/23010577

Abstract