Referenced in: none

Automatically associated channels: Cav1.1

Title: Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a Chinese family.

Authors: Qiufen Wang, Mugen Liu, Chunsheng Xu, Zhaohui Tang, Yuhua Liao, Rong Du, Wei Li, Xiaoyan Wu, Xu Wang, Ping Liu, Xianqin Zhang, Jianfang Zhu, Xiang Ren, Tie Ke, Qing Wang, Junguo Yang

Journal, date & volume: J. Mol. Med., 2005 Mar , 83, 203-8

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/15726306

Abstract