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295 related items for PubMed ID: 8603863

  • 1. Nonallelism of erd and prcd and exclusion of the canine RDS/peripherin gene as a candidate for both retinal degeneration loci.
    Ray K, Acland GM, Aguirre GD.
    Invest Ophthalmol Vis Sci; 1996 Apr; 37(5):783-94. PubMed ID: 8603863
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  • 2. Canine rod transducin alpha-1: cloning of the cDNA and evaluation of the gene as a candidate for progressive retinal atrophy.
    Ray K, Baldwin VJ, Zeiss C, Acland GM, Aguirre GD.
    Curr Eye Res; 1997 Jan; 16(1):71-7. PubMed ID: 9043826
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  • 3. Cosegregation of codon 807 mutation of the canine rod cGMP phosphodiesterase beta gene and rcd1.
    Ray K, Baldwin VJ, Acland GM, Blanton SH, Aguirre GD.
    Invest Ophthalmol Vis Sci; 1994 Dec; 35(13):4291-9. PubMed ID: 8002249
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  • 4. Evaluation of RDS/Peripherin and ROM1 as candidate genes in generalised progressive retinal atrophy and exclusion of digenic inheritance.
    Runte M, Dekomien G, Epplen JT.
    Anim Genet; 2000 Jun; 31(3):223-7. PubMed ID: 10895316
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  • 5. A peripherin/retinal degeneration slow mutation (Pro-210-Arg) associated with macular and peripheral retinal degeneration.
    Gorin MB, Jackson KE, Ferrell RE, Sheffield VC, Jacobson SG, Gass JD, Mitchell E, Stone EM.
    Ophthalmology; 1995 Feb; 102(2):246-55. PubMed ID: 7862413
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  • 6. Autosomal dominant cone-rod dystrophy associated with a Val200Glu mutation of the peripherin/RDS gene.
    Nakazawa M, Naoi N, Wada Y, Nakazaki S, Maruiwa F, Sawada A, Tamai M.
    Retina; 1996 Feb; 16(5):405-10. PubMed ID: 8912967
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  • 13. Linkage analysis and comparative mapping of canine progressive rod-cone degeneration (prcd) establishes potential locus homology with retinitis pigmentosa (RP17) in humans.
    Acland GM, Ray K, Mellersh CS, Gu W, Langston AA, Rine J, Ostrander EA, Aguirre GD.
    Proc Natl Acad Sci U S A; 1998 Mar 17; 95(6):3048-53. PubMed ID: 9501213
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  • 14. Peripherin/RDS gene mutation (Pro210Leu) and polymorphisms in Japanese patients with retinal dystrophies.
    Budu, Hayasaka S, Matsumoto M, Yamada T, Zhang XY, Hayasaka Y.
    Jpn J Ophthalmol; 2001 Mar 17; 45(4):355-8. PubMed ID: 11485765
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  • 15. Clinical features of a previously undescribed codon 216 (proline to serine) mutation in the peripherin/retinal degeneration slow gene in autosomal dominant retinitis pigmentosa.
    Fishman GA, Stone E, Gilbert LD, Vandenburgh K, Sheffield VC, Heckenlively JR.
    Ophthalmology; 1994 Aug 17; 101(8):1409-21. PubMed ID: 8058286
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  • 16. Splice site mutation in the peripherin/RDS gene associated with pattern dystrophy of the retina.
    Sears JE, Aaberg TA, Daiger SP, Moshfeghi DM.
    Am J Ophthalmol; 2001 Nov 17; 132(5):693-9. PubMed ID: 11704030
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  • 17. Cloning and characterization of canine SHARP1 and its evaluation as a positional candidate for canine early retinal degeneration (erd).
    Kukekova AV, Aguirre GD, Acland GM.
    Gene; 2003 Jul 17; 312():335-43. PubMed ID: 12909371
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  • 18. A null mutation in the human peripherin/RDS gene in a family with autosomal dominant retinitis punctata albescens.
    Kajiwara K, Sandberg MA, Berson EL, Dryja TP.
    Nat Genet; 1993 Mar 17; 3(3):208-12. PubMed ID: 8485575
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