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Journal Abstract Search

196 related items for PubMed ID: 9020843

  • 1. Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness.
    Yamamoto S, Sippel KC, Berson EL, Dryja TP.
    Nat Genet; 1997 Feb; 15(2):175-8. PubMed ID: 9020843
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  • 2. A homozygous 1-base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanese.
    Fuchs S, Nakazawa M, Maw M, Tamai M, Oguchi Y, Gal A.
    Nat Genet; 1995 Jul; 10(3):360-2. PubMed ID: 7670478
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  • 3. A novel homozygous GRK1 mutation (P391H) in 2 siblings with Oguchi disease with markedly reduced cone responses.
    Hayashi T, Gekka T, Takeuchi T, Goto-Omoto S, Kitahara K.
    Ophthalmology; 2007 Jan; 114(1):134-41. PubMed ID: 17070587
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  • 4. Evaluation of the human arrestin gene in patients with retinitis pigmentosa and stationary night blindness.
    Sippel KC, DeStefano JD, Berson EL, Dryja TP.
    Invest Ophthalmol Vis Sci; 1998 Mar; 39(3):665-70. PubMed ID: 9501883
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  • 5. [Molecular genetic study of congenital stationary night blindness].
    Nakamura M, Miyake Y.
    Nippon Ganka Gakkai Zasshi; 2004 Nov; 108(11):665-73. PubMed ID: 15584351
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  • 8. Increased susceptibility to light damage in an arrestin knockout mouse model of Oguchi disease (stationary night blindness).
    Chen J, Simon MI, Matthes MT, Yasumura D, LaVail MM.
    Invest Ophthalmol Vis Sci; 1999 Nov; 40(12):2978-82. PubMed ID: 10549660
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  • 11. A variant form of Oguchi disease mapped to 13q34 associated with partial deletion of GRK1 gene.
    Zhang Q, Zulfiqar F, Riazuddin SA, Xiao X, Yasmeen A, Rogan PK, Caruso R, Sieving PA, Riazuddin S, Hejtmancik JF.
    Mol Vis; 2005 Nov 14; 11():977-85. PubMed ID: 16319817
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  • 12. Novel mutations in the arrestin gene and associated clinical features in Japanese patients with Oguchi's disease.
    Nakamura M, Yamamoto S, Okada M, Ito S, Tano Y, Miyake Y.
    Ophthalmology; 2004 Jul 14; 111(7):1410-4. PubMed ID: 15234147
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  • 14. Gene analysis and evaluation of the single founder effect in Japanese patients with Oguchi disease.
    Saga M, Mashima Y, Kudoh J, Oguchi Y, Shimizu N.
    Jpn J Ophthalmol; 2004 Jul 14; 48(4):350-2. PubMed ID: 15295660
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  • 16. Macular Dysfunction in Oguchi Disease with the Frequent Mutation 1147delA in the SAG Gene.
    Hayashi T, Tsuzuranuki S, Kozaki K, Urashima M, Tsuneoka H.
    Ophthalmic Res; 2011 Oct 14; 46(4):175-80. PubMed ID: 21447990
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  • 17. A Chinese family with Oguchi's disease due to compound heterozygosity including a novel deletion in the arrestin gene.
    Huang L, Li W, Tang W, Zhu X, Ou-Yang P, Lu G.
    Mol Vis; 2012 Oct 14; 18():528-36. PubMed ID: 22419846
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  • 20. Genetic analysis and clinical features of three Chinese patients with Oguchi disease.
    Wei X, Li H, Wu S, Zhu T, Sui R.
    Doc Ophthalmol; 2023 Feb 14; 146(1):17-32. PubMed ID: 36417138
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