Referenced in: none

Automatically associated channels: Cav1.4 , Kv2.1 , Slo1

Title: Congenital stationary night blindness type 2 mutations S229P, G369D, L1068P, and W1440X alter channel gating or functional expression of Ca(v)1.4 L-type Ca2+ channels.

Authors: Jean-Charles Hoda, Francesca Zaghetto, Alexandra Koschak, Jörg Striessnig

Journal, date & volume: J. Neurosci., 2005 Jan 5 , 25, 252-9

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/15634789

Abstract