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Journal Abstract Search

239 related items for PubMed ID: 9804152

  • 21.
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  • 22. Increased sensitivity to light-induced damage in a mouse model of autosomal dominant retinal disease.
    White DA, Fritz JJ, Hauswirth WW, Kaushal S, Lewin AS.
    Invest Ophthalmol Vis Sci; 2007 May; 48(5):1942-51. PubMed ID: 17460245
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  • 24. Oscillatory potentials and pattern electroretinogram: are they related?
    Litao RE, Miyake Y, Yagasaki K.
    Jpn J Ophthalmol; 1986 May; 30(4):402-8. PubMed ID: 3495681
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  • 29. Congenital stationary night blindness: an animal model.
    Witzel DA, Smith EL, Wilson RD, Aguirre GD.
    Invest Ophthalmol Vis Sci; 1978 Aug; 17(8):788-95. PubMed ID: 308060
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  • 30. The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.
    Pusch CM, Zeitz C, Brandau O, Pesch K, Achatz H, Feil S, Scharfe C, Maurer J, Jacobi FK, Pinckers A, Andreasson S, Hardcastle A, Wissinger B, Berger W, Meindl A.
    Nat Genet; 2000 Nov; 26(3):324-7. PubMed ID: 11062472
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  • 31. Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness.
    Bech-Hansen NT, Naylor MJ, Maybaum TA, Pearce WG, Koop B, Fishman GA, Mets M, Musarella MA, Boycott KM.
    Nat Genet; 1998 Jul; 19(3):264-7. PubMed ID: 9662400
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  • 34. Investigations of photoreceptor synaptic transmission and light adaptation in the zebrafish visual mutant nrc.
    Van Epps HA, Yim CM, Hurley JB, Brockerhoff SE.
    Invest Ophthalmol Vis Sci; 2001 Mar; 42(3):868-74. PubMed ID: 11222552
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  • 37. Molecular genetics of Oguchi disease, fundus albipunctatus, and other forms of stationary night blindness: LVII Edward Jackson Memorial Lecture.
    Dryja TP.
    Am J Ophthalmol; 2000 Nov; 130(5):547-63. PubMed ID: 11078833
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