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Journal Abstract Search

392 related items for PubMed ID: 15381243

  • 1. Tyrosinase gene analysis in Japanese patients with oculocutaneous albinism.
    Goto M, Sato-Matsumura KC, Sawamura D, Yokota K, Nakamura H, Shimizu H.
    J Dermatol Sci; 2004 Sep; 35(3):215-20. PubMed ID: 15381243
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  • 3. Insertion/deletion mutations of type I oculocutaneous albinism in chinese patients from Taiwan.
    Tsai CH, Tsai FJ, Wu JY, Lin SP, Chang JG, Yang CF, Lee CC.
    Hum Mutat; 1999 Dec; 14(6):542. PubMed ID: 10571953
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  • 4. Tyrosinase gene mutations in type I (tyrosinase-deficient) oculocutaneous albinism define two clusters of missense substitutions.
    Tripathi RK, Strunk KM, Giebel LB, Weleber RG, Spritz RA.
    Am J Med Genet; 1992 Jul 15; 43(5):865-71. PubMed ID: 1642278
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  • 8. OCA1 in different ethnic groups of india is primarily due to founder mutations in the tyrosinase gene.
    Chaki M, Sengupta M, Mukhopadhyay A, Subba Rao I, Majumder PP, Das M, Samanta S, Ray K.
    Ann Hum Genet; 2006 Sep 15; 70(Pt 5):623-30. PubMed ID: 16907708
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  • 9. Higher prevalence of OCA1 in an ethnic group of eastern India is due to a founder mutation in the tyrosinase gene.
    Chaki M, Mukhopadhyay A, Chatterjee S, Das M, Samanta S, Ray K.
    Mol Vis; 2005 Jul 19; 11():531-4. PubMed ID: 16056219
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  • 10. Electron microscopic DOPA reaction test for oculocutaneous albinism.
    Takizawa Y, Kato S, Matsunaga J, Aozaki R, Tomita Y, Nishikawa T, Shimizu H.
    Arch Dermatol Res; 2000 Jun 19; 292(6):301-5. PubMed ID: 10929771
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  • 12. Genetic analysis of oculocutaneous albinism type 1 (OCA1) in Indian families: two novel frameshift mutations in the TYR Gene.
    Sundaresan P, Sil AK, Philp AR, Randolph MA, Natchiar G, Namperumalsamy P.
    Mol Vis; 2004 Dec 27; 10():1005-10. PubMed ID: 15635296
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