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602 related items for PubMed ID: 3393536

  • 1. Diverse point mutations in the human glucose-6-phosphate dehydrogenase gene cause enzyme deficiency and mild or severe hemolytic anemia.
    Vulliamy TJ, D'Urso M, Battistuzzi G, Estrada M, Foulkes NS, Martini G, Calabro V, Poggi V, Giordano R, Town M.
    Proc Natl Acad Sci U S A; 1988 Jul; 85(14):5171-5. PubMed ID: 3393536
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  • 2. Several mutations including two novel mutations of the glucose-6-phosphate dehydrogenase gene in Polish G6PD deficient subjects with chronic nonspherocytic hemolytic anemia, acute hemolytic anemia, and favism.
    Jablonska-Skwiecinska E, Lewandowska I, Plochocka D, Topczewski J, Zimowski JG, Klopocka J, Burzynska B.
    Hum Mutat; 1999 Jul; 14(6):477-84. PubMed ID: 10571945
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  • 3. Favism, the commonest form of severe hemolytic anemia in Palestinian children, varies in severity with three different variants of G6PD deficiency within the same community.
    Reading NS, Sirdah MM, Shubair ME, Nelson BE, Al-Kahlout MS, Al-Tayeb JM, Aboud LN, Shaban MA, Luzzatto L, Prchal JT.
    Blood Cells Mol Dis; 2016 Sep; 60():58-64. PubMed ID: 27519946
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  • 7. At least five polymorphic mutants account for the prevalence of glucose-6-phosphate dehydrogenase deficiency in Algeria.
    Nafa K, Reghis A, Osmani N, Baghli L, Aït-Abbes H, Benabadji M, Kaplan JC, Vulliamy T, Luzzatto L.
    Hum Genet; 1994 Nov; 94(5):513-7. PubMed ID: 7959686
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  • 8. G6PD Ferrara I has the same two mutations as G6PD A(-) but a distinct biochemical phenotype.
    Cappellini MD, Sampietro M, Toniolo D, Carandina G, Martinez di Montemuros F, Tavazzi D, Fiorelli G.
    Hum Genet; 1994 Feb; 93(2):139-42. PubMed ID: 7906668
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  • 15. Identification of two novel deletion mutations in glucose-6-phosphate dehydrogenase gene causing hemolytic anemia.
    Hirono A, Fujii H, Miwa S.
    Blood; 1995 Feb 15; 85(4):1118-21. PubMed ID: 7849299
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  • 17. Multiple glucose 6-phosphate dehydrogenase-deficient variants correlate with malaria endemicity in the Vanuatu archipelago (southwestern Pacific).
    Ganczakowski M, Town M, Bowden DK, Vulliamy TJ, Kaneko A, Clegg JB, Weatherall DJ, Luzzatto L.
    Am J Hum Genet; 1995 Jan 15; 56(1):294-301. PubMed ID: 7825590
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  • 20. Glucose-6-phosphate dehydrogenase (G6PD) deficiency in southern Italy: a case of G6PD A(-) associated with favism.
    Calabrò V, Cascone A, Malaspina P, Battistuzzi G.
    Haematologica; 1989 Jan 15; 74(1):71-3. PubMed ID: 2498187
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