Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram.
Zeitz C, van Genderen M, Neidhardt J, Luhmann UF, Hoeben F, Forster U, Wycisk K, Mátyás G, Hoyng CB, Riemslag F, Meire F, Cremers FP, Berger W.
Invest Ophthalmol Vis Sci. 2005 Nov;46(11):4328-35.PMID: 16249515 [PubMed - indexed for MEDLINE]Related articlesFree article