Referenced in: none

Automatically associated channels: Cav1.4

Title: A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants.

Authors: K M Boycott, T A Maybaum, M J Naylor, R G Weleber, J Robitaille, Y Miyake, A A Bergen, M E Pierpont, W G Pearce, N T Bech-Hansen

Journal, date & volume: Hum. Genet., 2001 Feb , 108, 91-7

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/11281458

Abstract