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Journal Abstract Search

187 related items for PubMed ID: 1580841

  • 1. Ocular findings associated with a rhodopsin gene codon 106 mutation. Glycine-to-arginine change in autosomal dominant retinitis pigmentosa.
    Fishman GA, Stone EM, Gilbert LD, Sheffield VC.
    Arch Ophthalmol; 1992 May; 110(5):646-53. PubMed ID: 1580841
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  • 7. Autosomal dominant retinitis pigmentosa with a rhodopsin mutation (Arg-135-Trp). Disease phenotype in a Swedish family.
    Ponjavic V, Abrahamson M, Andréasson S, Ehinger B, Fex G.
    Acta Ophthalmol Scand; 1997 Apr; 75(2):218-23. PubMed ID: 9197578
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  • 10. Clinical features of autosomal dominant retinitis pigmentosa with rhodopsin gene codon 17 mutation and retinal neovascularization in a Japanese patient.
    Hayakawa M, Hotta Y, Imai Y, Fujiki K, Nakamura A, Yanashima K, Kanai A.
    Am J Ophthalmol; 1993 Feb 15; 115(2):168-73. PubMed ID: 7679248
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  • 13. Description of a new mutation in rhodopsin, Pro23Ala, and comparison with electroretinographic and clinical characteristics of the Pro23His mutation.
    Oh KT, Weleber RG, Lotery A, Oh DM, Billingslea AM, Stone EM.
    Arch Ophthalmol; 2000 Sep 15; 118(9):1269-76. PubMed ID: 10980774
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  • 20. Missense mutation of rhodopsin gene codon 15 found in Japanese autosomal dominant retinitis pigmentosa.
    Fujiki K, Hotta Y, Murakami A, Yoshii M, Hayakawa M, Ichikawa T, Takeda M, Akeo K, Okisaka S, Kanai A.
    Jpn J Hum Genet; 1995 Sep 15; 40(3):271-7. PubMed ID: 8527802
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