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Journal Abstract Search

122 related items for PubMed ID: 32953689

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  • 24. 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
    [Abstract] [Full Text] [Related]

  • 25. Rapid detection of SAG 926delA mutation using real-time polymerase chain reaction.
    Yoshida S, Yamaji Y, Yoshida A, Ikeda Y, Yamamoto K, Ishibashi T.
    Mol Vis; 2006 Dec 06; 12():1552-7. PubMed ID: 17200654
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  • 26. Oguchi disease masked by retinitis pigmentosa.
    Sonoyama H, Shinoda K, Ishigami C, Tada Y, Ideta H, Ideta R, Takahashi M, Miyake Y.
    Doc Ophthalmol; 2011 Oct 06; 123(2):127-33. PubMed ID: 21922265
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  • 29. 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 Oct 06; 48(4):350-2. PubMed ID: 15295660
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  • 30. Mizuo-Nakamura phenomenon in Oguchi disease due to a homozygous nonsense mutation in the SAG gene.
    Sergouniotis PI, Davidson AE, Sehmi K, Webster AR, Robson AG, Moore AT.
    Eye (Lond); 2011 Aug 06; 25(8):1098-101. PubMed ID: 21494281
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  • 31. Novel mutations in the GRK1 gene in Japanese patients With Oguchi disease.
    Oishi A, Akimoto M, Kawagoe N, Mandai M, Takahashi M, Yoshimura N.
    Am J Ophthalmol; 2007 Sep 06; 144(3):475-7. PubMed ID: 17765441
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  • 32. [Molecular genetic study of congenital stationary night blindness].
    Nakamura M, Miyake Y.
    Nippon Ganka Gakkai Zasshi; 2004 Nov 06; 108(11):665-73. PubMed ID: 15584351
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  • 34. Oguchi disease: suggestion of linkage to markers on chromosome 2q.
    Maw MA, John S, Jablonka S, Müller B, Kumaramanickavel G, Oehlmann R, Denton MJ, Gal A.
    J Med Genet; 1995 May 06; 32(5):396-8. PubMed ID: 7616550
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  • 35. Arrestin gene mutations in autosomal recessive retinitis pigmentosa.
    Nakazawa M, Wada Y, Tamai M.
    Arch Ophthalmol; 1998 Apr 06; 116(4):498-501. PubMed ID: 9565049
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  • 36. [Establishment of the concept of new clinical entities--complete and incomplete form of congenital stationary night blindness].
    Miyake Y.
    Nippon Ganka Gakkai Zasshi; 2002 Dec 06; 106(12):737-55; discussion 756. PubMed ID: 12610835
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  • 37. Oguchi disease with unusual findings associated with a heterozygous mutation in the SAG gene.
    Fujinami K, Tsunoda K, Nakamura M, Oguchi Y, Miyake Y.
    Arch Ophthalmol; 2011 Oct 06; 129(10):1375-6. PubMed ID: 21987685
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  • 39. Mizuo-Nakamura phenomenon in an Indian male.
    Agarwal R, Tripathy K, Bandyopadhyay G, Basu K.
    Clin Case Rep; 2019 Feb 06; 7(2):401-403. PubMed ID: 30847219
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