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43. 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. PubMed ID: 16249515 [TBL] [Abstract][Full Text] [Related]
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