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117 related items for PubMed ID: 9099845

  • 1. Oculocutaneous albinism (OCA2) in sub-Saharan Africa: distribution of the common 2.7-kb P gene deletion mutation.
    Stevens G, Ramsay M, Jenkins T.
    Hum Genet; 1997 Apr; 99(4):523-7. PubMed ID: 9099845
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  • 2. An intragenic deletion of the P gene is the common mutation causing tyrosinase-positive oculocutaneous albinism in southern African Negroids.
    Stevens G, van Beukering J, Jenkins T, Ramsay M.
    Am J Hum Genet; 1995 Mar; 56(3):586-91. PubMed ID: 7887411
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  • 4. Type 2 oculocutaneous albinism (OCA2) in Zimbabwe and Cameroon: distribution of the 2.7-kb deletion allele of the P gene.
    Puri N, Durbam-Pierre D, Aquaron R, Lund PM, King RA, Brilliant MH.
    Hum Genet; 1997 Oct; 100(5-6):651-6. PubMed ID: 9341887
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  • 7. Molecular genetic characterization of Congolese patients with oculocutaneous albinism.
    Laetitia MM, Veronique K, Mamy NZ, Cathy SM, Aimé L, Race V, Prosper LT, Devriendt K.
    Eur J Med Genet; 2022 Nov; 65(11):104611. PubMed ID: 36116698
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  • 9. In Southern Africa, brown oculocutaneous albinism (BOCA) maps to the OCA2 locus on chromosome 15q: P-gene mutations identified.
    Manga P, Kromberg J, Turner A, Jenkins T, Ramsay M.
    Am J Hum Genet; 2001 Mar; 68(3):782-7. PubMed ID: 11179026
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  • 10. Albinism and disease causing pathogens in Tanzania: are alleles that are associated with OCA2 being maintained by balancing selection?
    Tuli AM, Valenzuela RK, Kamugisha E, Brilliant MH.
    Med Hypotheses; 2012 Dec; 79(6):875-8. PubMed ID: 23063908
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  • 11. Oculocutaneous albinism in an isolated Tonga community in Zimbabwe.
    Lund PM, Puri N, Durham-Pierre D, King RA, Brilliant MH.
    J Med Genet; 1997 Sep; 34(9):733-5. PubMed ID: 9321758
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  • 13. A 122.5-kilobase deletion of the P gene underlies the high prevalence of oculocutaneous albinism type 2 in the Navajo population.
    Yi Z, Garrison N, Cohen-Barak O, Karafet TM, King RA, Erickson RP, Hammer MF, Brilliant MH.
    Am J Hum Genet; 2003 Jan; 72(1):62-72. PubMed ID: 12469324
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  • 15. Rufous oculocutaneous albinism in southern African Blacks is caused by mutations in the TYRP1 gene.
    Manga P, Kromberg JG, Box NF, Sturm RA, Jenkins T, Ramsay M.
    Am J Hum Genet; 1997 Nov; 61(5):1095-101. PubMed ID: 9345097
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  • 19. A nonsense nucleotide substitution in the oculocutaneous albinism II gene underlies the original pink-eyed dilution allele (Oca2(p)) in mice.
    Shoji H, Kiniwa Y, Okuyama R, Yang M, Higuchi K, Mori M.
    Exp Anim; 2015 Nov; 64(2):171-9. PubMed ID: 25736709
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  • 20. [Mutations and polymorphisms of the P gene associated with oculocutaneous albinism type II].
    Duan HL, Zheng H, Li HY.
    Yi Chuan; 2005 Nov; 27(6):984-8. PubMed ID: 16378950
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