Referenced in: none

Automatically associated channels: Cav1.1

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

Authors: Tie Ke, Cladelis Rubio Gomez, Heidi Eliana Mateus, Juan Andres Castano, Qing Kenneth Wang

Journal, date & volume: J. Hum. Genet., 2009 Nov , 54, 660-4

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/19779499

Abstract