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Journal Abstract Search

202 related items for PubMed ID: 11317367

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  • 2. [Mutation analysis of retinitis pigmentosa 1 gene in Chinese with retinitis pigmentosa].
    Zhang X, Yeung KY, Pang CP, Fu W.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Jun; 19(3):194-7. PubMed ID: 12048676
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  • 3. [Digenic association of RHO and RP1 genes with retinitis pigmentosa among Chinese population in Hong Kong].
    Wang DY, Fan BJ, Chan WM, Tam OS, Chiang WY, Lam SC, Pang CP.
    Zhonghua Yi Xue Za Zhi; 2005 Jun 22; 85(23):1613-7. PubMed ID: 16185528
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  • 4. Differential pattern of RP1 mutations in retinitis pigmentosa.
    Zhang X, Chen LJ, Law JP, Lai TY, Chiang SW, Tam PO, Chu KY, Wang N, Zhang M, Pang CP.
    Mol Vis; 2010 Jul 15; 16():1353-60. PubMed ID: 20664799
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  • 5. Screening for mutations in a novel retinal-specific gene among Chinese patients with retinitis pigmentosa.
    Xiaoli Z, Weiling F, Pang CP, Yeung KY.
    Chin Med Sci J; 2002 Dec 15; 17(4):225-30. PubMed ID: 12901510
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  • 6. Identification of a novel nonsense mutation in RP1 that causes autosomal recessive retinitis pigmentosa in an Indonesian family.
    Siemiatkowska AM, Astuti GD, Arimadyo K, den Hollander AI, Faradz SM, Cremers FP, Collin RW.
    Mol Vis; 2012 Dec 15; 18():2411-9. PubMed ID: 23077400
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  • 7. Three novel and the common Arg677Ter RP1 protein truncating mutations causing autosomal dominant retinitis pigmentosa in a Spanish population.
    Gamundi MJ, Hernan I, Martínez-Gimeno M, Maseras M, García-Sandoval B, Ayuso C, Antiñolo G, Baiget M, Carballo M.
    BMC Med Genet; 2006 Apr 05; 7():35. PubMed ID: 16597330
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  • 10. RP1 and autosomal dominant rod-cone dystrophy: novel mutations, a review of published variants, and genotype-phenotype correlation.
    Audo I, Mohand-Saïd S, Dhaenens CM, Germain A, Orhan E, Antonio A, Hamel C, Sahel JA, Bhattacharya SS, Zeitz C.
    Hum Mutat; 2012 Jan 05; 33(1):73-80. PubMed ID: 22052604
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  • 12. Association of NR2E3 but not NRL mutations with retinitis pigmentosa in the Chinese population.
    Yang Y, Zhang X, Chen LJ, Chiang SW, Tam PO, Lai TY, Chan CK, Wang N, Lam DS, Pang CP.
    Invest Ophthalmol Vis Sci; 2010 Apr 05; 51(4):2229-35. PubMed ID: 19933183
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  • 17. Identification of a novel homozygous nonsense mutation in EYS in a Chinese family with autosomal recessive retinitis pigmentosa.
    Huang Y, Zhang J, Li C, Yang G, Liu M, Wang QK, Tang Z.
    BMC Med Genet; 2010 Aug 10; 11():121. PubMed ID: 20696082
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  • 18. Variants of RP1 gene in Chinese patients with autosomal dominant retinitis pigmentosa.
    Sheng X, Zhang X, Wu W, Zhuang W, Meng R, Rong W.
    Can J Ophthalmol; 2008 Apr 10; 43(2):208-12. PubMed ID: 18347624
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