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31. Autosomal dominant congenital stationary night blindness and normal fundus with an electronegative electroretinogram. Noble KG, Carr RE, Siegel IM. Am J Ophthalmol; 1990 Jan 15; 109(1):44-8. PubMed ID: 2297031 [Abstract] [Full Text] [Related]
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34. A Japanese pedigree of autosomal dominant congenital stationary night blindness with variable expressivity. Hayakawa M, Imai Y, Wakita M, Kato K, Yanashima K, Miyake Y, Kanai A. Ophthalmic Paediatr Genet; 1992 Dec 15; 13(4):211-7. PubMed ID: 1488221 [Abstract] [Full Text] [Related]
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39. Slow and fast rod ERG pathways in patients with X-linked complete stationary night blindness carrying mutations in the NYX gene. Scholl HP, Langrová H, Pusch CM, Wissinger B, Zrenner E, Apfelstedt-Sylla E. Invest Ophthalmol Vis Sci; 2001 Oct 15; 42(11):2728-36. PubMed ID: 11581222 [Abstract] [Full Text] [Related]
40. Congenital stationary night blindness: an animal model. Witzel DA, Smith EL, Wilson RD, Aguirre GD. Invest Ophthalmol Vis Sci; 1978 Aug 15; 17(8):788-95. PubMed ID: 308060 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]