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Journal Abstract Search

334 related items for PubMed ID: 25078356

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  • 6. Visual Outcomes in Japanese Patients with Retinitis Pigmentosa and Usher Syndrome Caused by USH2A Mutations.
    Nagase Y, Kurata K, Hosono K, Suto K, Hikoya A, Nakanishi H, Mizuta K, Mineta H, Minoshima S, Hotta Y.
    Semin Ophthalmol; 2018; 33(4):560-565. PubMed ID: 28678594
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  • 10. Novel USH2A compound heterozygous mutations cause RP/USH2 in a Chinese family.
    Liu X, Tang Z, Li C, Yang K, Gan G, Zhang Z, Liu J, Jiang F, Wang Q, Liu M.
    Mol Vis; 2010 Mar 17; 16():454-61. PubMed ID: 20309401
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  • 11. Identification of 13 novel USH2A mutations in Chinese retinitis pigmentosa and Usher syndrome patients by targeted next-generation sequencing.
    Qu LH, Jin X, Long YL, Ren JY, Weng CH, Xu HW, Liu Y, Meng XH, Li SY, Yin ZQ.
    Biosci Rep; 2020 Jan 31; 40(1):. PubMed ID: 31904091
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  • 12. Mutation analysis in the long isoform of USH2A in American patients with Usher Syndrome type II.
    Yan D, Ouyang X, Patterson DM, Du LL, Jacobson SG, Liu XZ.
    J Hum Genet; 2009 Dec 31; 54(12):732-8. PubMed ID: 19881469
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  • 13. Mutation screening of the USH2A gene in retinitis pigmentosa and USHER patients in a Han Chinese population.
    Huang L, Mao Y, Yang J, Li Y, Li Y, Yang Z.
    Eye (Lond); 2018 Oct 31; 32(10):1608-1614. PubMed ID: 29899460
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  • 15. Comprehensive screening of the USH2A gene in Usher syndrome type II and non-syndromic recessive retinitis pigmentosa.
    Seyedahmadi BJ, Rivolta C, Keene JA, Berson EL, Dryja TP.
    Exp Eye Res; 2004 Aug 31; 79(2):167-73. PubMed ID: 15325563
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  • 16. Genetic characteristics of retinitis pigmentosa in 1204 Japanese patients.
    Koyanagi Y, Akiyama M, Nishiguchi KM, Momozawa Y, Kamatani Y, Takata S, Inai C, Iwasaki Y, Kumano M, Murakami Y, Omodaka K, Abe T, Komori S, Gao D, Hirakata T, Kurata K, Hosono K, Ueno S, Hotta Y, Murakami A, Terasaki H, Wada Y, Nakazawa T, Ishibashi T, Ikeda Y, Kubo M, Sonoda KH.
    J Med Genet; 2019 Oct 31; 56(10):662-670. PubMed ID: 31213501
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  • 18. USH2A mutational spectrum causing syndromic and non-syndromic retinal dystrophies in a large cohort of Mexican patients.
    Ordoñez-Labastida V, Chacon-Camacho OF, Lopez-Rodriguez VR, Zenteno JC.
    Mol Vis; 2023 Oct 31; 29():31-38. PubMed ID: 37287646
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  • 19. Whole exome sequencing identifies novel USH2A mutations and confirms Usher syndrome 2 diagnosis in Chinese retinitis pigmentosa patients.
    Ng TK, Tang W, Cao Y, Chen S, Zheng Y, Xiao X, Chen H.
    Sci Rep; 2019 Apr 04; 9(1):5628. PubMed ID: 30948794
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