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Journal Abstract Search

133 related items for PubMed ID: 34162253

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  • 2. A compound heterozygous mutation in the S-Antigen Visual Arrestin SAG gene in a Chinese patient with Oguchi type one: a case report.
    Deng Z, Fan F, Tang D, Wu Y, Shu Y, Wu K.
    BMC Ophthalmol; 2022 Mar 04; 22(1):99. PubMed ID: 35246075
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  • 4. 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 04; 146(1):17-32. PubMed ID: 36417138
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  • 7. Mutation analysis reveals novel and known mutations in SAG gene in first two Egyptian families with Oguchi disease.
    Tawfik CA, Elbagoury NM, Khater NI, Essawi ML.
    BMC Ophthalmol; 2022 May 12; 22(1):217. PubMed ID: 35549688
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  • 10. Oguchi disease caused by a homozygous novel SAG splicing alteration associated with the multiple evanescent white dot syndrome: A 15-month follow-up.
    Liu X, Gao L, Wang G, Long Y, Ren J, Fujinami K, Meng X, Li S.
    Doc Ophthalmol; 2020 Dec 12; 141(3):217-226. PubMed ID: 32333190
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  • 12. 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 12; 46(4):175-80. PubMed ID: 21447990
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  • 15. Retinal findings in a patient of French ancestry with CABP4-related retinal disease.
    Smirnov VM, Zeitz C, Soumittra N, Audo I, Defoort-Dhellemmes S.
    Doc Ophthalmol; 2018 Apr 12; 136(2):135-143. PubMed ID: 29525873
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  • 16. A Homozygote Mutation in S-Antigen Visual Arrestin SAG Gene in an Iranian Patient with Oguchi Type One: A Case Report.
    Aryan H, Bahadori A, Farhud DD, Zarif Yeganeh M, Pourkalhor H.
    Iran J Public Health; 2020 May 12; 49(5):995-1000. PubMed ID: 32953689
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  • 18. Oguchi type I caused by a homozygous missense variation in the SAG gene.
    Colombo L, Abeshi A, Maltese PE, Frecer V, Miertuš J, Cerra D, Bertelli M, Rossetti L.
    Eur J Med Genet; 2019 Sep 12; 62(9):103548. PubMed ID: 30267901
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