Referenced in: none

Automatically associated channels: Kir2.1

Title: Novel KCNJ2 mutation in familial periodic paralysis with ventricular dysrhythmia.

Authors: Tomohiko Ai, Yuichiro Fujiwara, Keiko Tsuji, Hideo Otani, Shozo Nakano, Yoshihiro Kubo, Minoru Horie

Journal, date & volume: Circulation, 2002 Jun 4 , 105, 2592-4

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/12045162

Abstract