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49. A form of congenital stationary night blindness with apparent defect of rod phototransduction. Peachey NS, Fishman GA, Kilbride PE, Alexander KR, Keehan KM, Derlacki DJ. Invest Ophthalmol Vis Sci; 1990 Feb; 31(2):237-46. PubMed ID: 2303327 [Abstract] [Full Text] [Related]
55. The photopic electroretinogram in congenital stationary night blindness with myopia. Lachapelle P, Little JM, Polomeno RC. Invest Ophthalmol Vis Sci; 1983 Apr; 24(4):442-50. PubMed ID: 6601088 [Abstract] [Full Text] [Related]
56. Mutations in NYX of individuals with high myopia, but without night blindness. Zhang Q, Xiao X, Li S, Jia X, Yang Z, Huang S, Caruso RC, Guan T, Sergeev Y, Guo X, Hejtmancik JF. Mol Vis; 2007 Mar 01; 13():330-6. PubMed ID: 17392683 [Abstract] [Full Text] [Related]
58. Aland Island eye disease (Forsius-Eriksson syndrome) associated with contiguous deletion syndrome at Xp21. Similarity to incomplete congenital stationary night blindness. Weleber RG, Pillers DA, Powell BR, Hanna CE, Magenis RE, Buist NR. Arch Ophthalmol; 1989 Aug 01; 107(8):1170-9. PubMed ID: 2667510 [Abstract] [Full Text] [Related]
59. A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants. Boycott KM, Maybaum TA, Naylor MJ, Weleber RG, Robitaille J, Miyake Y, Bergen AA, Pierpont ME, Pearce WG, Bech-Hansen NT. Hum Genet; 2001 Feb 01; 108(2):91-7. PubMed ID: 11281458 [Abstract] [Full Text] [Related]