Referenced in: none

Automatically associated channels: Cav1.1

Title: Identification of mutations in the CACNL1A3 gene in 13 families of Scandinavian origin having hypokalemic periodic paralysis and evidence of a founder effect in Danish families.

Authors: A Sillén, T Sørensen, I Kantola, M L Friis, K H Gustavson, C Wadelius

Journal, date & volume: Am. J. Med. Genet., 1997 Mar 3 , 69, 102-6

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/9066893

Abstract