PubMed 9662400
Referenced in: none
Automatically associated channels: Cav1.4
Title: Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness.
Authors: N T Bech-Hansen, M J Naylor, T A Maybaum, W G Pearce, B Koop, G A Fishman, M Mets, M A Musarella, K M Boycott
Journal, date & volume: Nat. Genet., 1998 Jul , 19, 264-7
PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/9662400
Abstract