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76 related items for PubMed ID: 1581693

  • 1.
    ; . PubMed ID:
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  • 2. A mild phenotype of autosomal dominant retinitis pigmentosa is associated with the rhodopsin mutation Pro-267-Leu.
    Ponjavic V, Abrahamson M, Andréasson S, Ehinger B, Fex G, Polland W.
    Ophthalmic Genet; 1997 Jun; 18(2):63-70. PubMed ID: 9228242
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  • 3. Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa.
    Kajiwara K, Hahn LB, Mukai S, Travis GH, Berson EL, Dryja TP.
    Nature; 1991 Dec 12; 354(6353):480-3. PubMed ID: 1684223
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  • 5. Autosomal dominant retinitis pigmentosa caused by the threonine-17-methionine rhodopsin mutation: retinal histopathology and immunocytochemistry.
    Li ZY, Jacobson SG, Milam AH.
    Exp Eye Res; 1994 Apr 12; 58(4):397-408. PubMed ID: 7925677
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  • 7. Ser186Pro mutation of RHO gene in a Spanish autosomal dominant retinitis pigmentosa (ADRP) family.
    Trujillo MJ, Garcia-Sandoval B, Lorda-Sanchez I, Gimenez A, Sanz R, Rodriguez de Alba M, Gonzalez-Gonzalez MC, Ibañez A, Ramos C, Ayuso C.
    Ophthalmic Genet; 2000 Dec 12; 21(4):251-6. PubMed ID: 11135497
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  • 8. [Genetic heterogeneity of retinitis pigmentosa].
    Krawczyński MR, Pecold K.
    Klin Oczna; 1994 Jan 12; 96(1):24-9. PubMed ID: 8078270
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  • 12. [Screening of candidate genes in a family with autosomal dominant retinitis pigmentosa].
    Teng Y, Tian H, Wang H, Hu X, Chen Y, Yang Z, Wang W.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Apr 12; 20(2):164-6. PubMed ID: 12673590
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  • 13. [Mutations of the rhodopsin gene and their phenotypic effects].
    Hübner H, Brzeziańska E.
    Postepy Hig Med Dosw; 1994 Apr 12; 48(6):677-88. PubMed ID: 7675729
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  • 14. [Retinitis pigmentosa--clinical and genetic aspects with low vision].
    Bogdănici C, Rusu C, Moţoc I, Crăşmaru C.
    Oftalmologia; 2008 Apr 12; 52(2):64-71. PubMed ID: 19065917
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  • 15. Phenotype of autosomal dominant cone-rod dystrophy due to the R838C mutation of the GUCY2D gene encoding retinal guanylate cyclase-1.
    Smith M, Whittock N, Searle A, Croft M, Brewer C, Cole M.
    Eye (Lond); 2007 Sep 12; 21(9):1220-5. PubMed ID: 17041576
    [Abstract] [Full Text] [Related]

  • 16. A point mutation of the rhodopsin gene in one form of retinitis pigmentosa.
    Dryja TP, McGee TL, Reichel E, Hahn LB, Cowley GS, Yandell DW, Sandberg MA, Berson EL.
    Nature; 1990 Jan 25; 343(6256):364-6. PubMed ID: 2137202
    [Abstract] [Full Text] [Related]

  • 17. Genetic and clinical characterization of a survey population with retinitis pigmentosa.
    Boughman JA, Caldwell RJ.
    Prog Clin Biol Res; 1982 Jan 25; 82():147-66. PubMed ID: 7111271
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  • 18. Clinical features and mutations in patients with dominant retinitis pigmentosa-1 (RP1).
    Berson EL, Grimsby JL, Adams SM, McGee TL, Sweklo E, Pierce EA, Sandberg MA, Dryja TP.
    Invest Ophthalmol Vis Sci; 2001 Sep 25; 42(10):2217-24. PubMed ID: 11527933
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  • 19. Acuity recovery and cone pigment regeneration after a bleach in patients with retinitis pigmentosa and rhodopsin mutations.
    Sandberg MA, Pawlyk BS, Berson EL.
    Invest Ophthalmol Vis Sci; 1999 Sep 25; 40(10):2457-61. PubMed ID: 10476820
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  • 20. A brief review of retinitis pigmentosa and the identified retinitis pigmentosa genes.
    Phelan JK, Bok D.
    Mol Vis; 2000 Jul 08; 6():116-24. PubMed ID: 10889272
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