Referenced in: none

Automatically associated channels: Kv8.2

Title: Long-term follow-up of the human phenotype in three siblings with cone dystrophy associated with a homozygous p.G461R mutation of KCNV2.

Authors: Christoph Friedburg, Bernd Wissinger, Maria Schambeck, Michael Bonin, Susanne Kohl, Birgit Lorenz

Journal, date & volume: Invest. Ophthalmol. Vis. Sci., 2011 Nov , 52, 8621-9

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/21911584

Abstract