Referenced in: none

Automatically associated channels: Cav1.4 , Slo1

Title: Functional analysis of congenital stationary night blindness type-2 CACNA1F mutations F742C, G1007R, and R1049W.

Authors: J B Peloquin, R Rehak, C J Doering, J E McRory

Journal, date & volume: Neuroscience, 2007 Dec 5 , 150, 335-45

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/17949918

Abstract