Referenced in: none

Automatically associated channels: Cav1.1

Title: Hypokalemic periodic paralysis and mutations in the CACNL1A3 gene: case study in a Japanese family.

Authors: T Wada, A Yachie, S Fujita, K Takei, R Sumita, T Ichihara, S Koizumi

Journal, date & volume: Pediatr Int, 2000 Jun , 42, 325-7

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/10881598

Abstract