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Journal Abstract Search

143 related items for PubMed ID: 16185528

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  • 2. RP1 in Chinese: Eight novel variants and evidence that truncation of the extreme C-terminal does not cause retinitis pigmentosa.
    Baum L, Chan WM, Yeung KY, Lam DS, Kwok AK, Pang CP.
    Hum Mutat; 2001 May; 17(5):436. PubMed ID: 11317367
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  • 3. Microarray-based mutation detection and phenotypic characterization in Korean patients with retinitis pigmentosa.
    Kim C, Kim KJ, Bok J, Lee EJ, Kim DJ, Oh JH, Park SP, Shin JY, Lee JY, Yu HG.
    Mol Vis; 2012 May; 18():2398-410. PubMed ID: 23049240
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  • 4. [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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  • 6. Compound heterozygosity of two novel truncation mutations in RP1 causing autosomal recessive retinitis pigmentosa.
    Chen LJ, Lai TY, Tam PO, Chiang SW, Zhang X, Lam S, Lai RY, Lam DS, Pang CP.
    Invest Ophthalmol Vis Sci; 2010 Apr; 51(4):2236-42. PubMed ID: 19933189
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  • 10. 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; 51(4):2229-35. PubMed ID: 19933183
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  • 12. 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; 43(2):208-12. PubMed ID: 18347624
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  • 13. A molecular case report of autosomal dominant retinitis pigmentosa: RP1/RHO sequence variants in a Turkish family.
    Nalbantoglu SM, Shahbazov C, Berdeli A.
    OMICS; 2012 Apr; 16(1-2):18-23. PubMed ID: 22321012
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  • 16. De novo mutation in the RP1 gene (Arg677ter) associated with retinitis pigmentosa.
    Schwartz SB, Aleman TS, Cideciyan AV, Swaroop A, Jacobson SG, Stone EM.
    Invest Ophthalmol Vis Sci; 2003 Aug; 44(8):3593-7. PubMed ID: 12882812
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  • 18. 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; 17(4):225-30. PubMed ID: 12901510
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  • 19. A novel missense RP1 mutation in retinitis pigmentosa.
    Chiang SW, Wang DY, Chan WM, Tam PO, Chong KK, Lam DS, Pang CP.
    Eye (Lond); 2006 May; 20(5):602-5. PubMed ID: 15933747
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  • 20. Spectrum of rhodopsin mutations in Korean patients with retinitis pigmentosa.
    Kim KJ, Kim C, Bok J, Kim KS, Lee EJ, Park SP, Chung H, Han BG, Kim HL, Kimm K, Yu HG, Lee JY.
    Mol Vis; 2011 May; 17():844-53. PubMed ID: 21677794
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