Referenced in: none

Automatically associated channels: Cav1.1 , Nav1.4

Title: [The mutation R672H in SCN4A gene exists in Chinese patients with hypokalaemic periodic paralysis]

Authors: Qing Ke, Quan-gang Xu, De-hui Huang, Hui-jun Yuan, Ya-li Zhao, Wei-ping Wu

Journal, date & volume: Zhonghua Yi Xue Za Zhi, 2006 Mar 21 , 86, 724-7

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/16681942

Abstract