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22. CNGB3 achromatopsia with progressive loss of residual cone function and impaired rod-mediated function. Khan NW; Wissinger B; Kohl S; Sieving PA Invest Ophthalmol Vis Sci; 2007 Aug; 48(8):3864-71. PubMed ID: 17652762 [TBL] [Abstract][Full Text] [Related]
23. [The characteristic electroretinogram anomalies in age-related macular degeneration]. Wu LZ Zhonghua Yan Ke Za Zhi; 1991 Jul; 27(4):197-9. PubMed ID: 1935441 [TBL] [Abstract][Full Text] [Related]
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30. Symptomatic abnormalities of dark adaptation in patients with EFEMP1 retinal dystrophy (Malattia Leventinese/Doyne honeycomb retinal dystrophy). Haimovici R; Wroblewski J; Piguet B; Fitzke FW; Holder GE; Arden GB; Bird AC Eye (Lond); 2002 Jan; 16(1):7-15. PubMed ID: 11913893 [TBL] [Abstract][Full Text] [Related]
32. Association of acquired color vision defects in blue cone monochromatism. Terasaki H; Miyake Y Jpn J Ophthalmol; 1995; 39(1):55-9. PubMed ID: 7643484 [TBL] [Abstract][Full Text] [Related]
34. Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2. Wissinger B; Dangel S; Jägle H; Hansen L; Baumann B; Rudolph G; Wolf C; Bonin M; Koeppen K; Ladewig T; Kohl S; Zrenner E; Rosenberg T Invest Ophthalmol Vis Sci; 2008 Feb; 49(2):751-7. PubMed ID: 18235024 [TBL] [Abstract][Full Text] [Related]
35. Color vision defects in retinal disease. MacKay CJ Arch Ophthalmol; 1989 Jun; 107(6):790-1. PubMed ID: 2786407 [No Abstract] [Full Text] [Related]
36. Spectral characteristics of electroretinography in congenital red-green color blindness. Uji Y Jpn J Ophthalmol; 1987; 31(1):61-80. PubMed ID: 3498068 [TBL] [Abstract][Full Text] [Related]
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