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Journal Abstract Search

181 related items for PubMed ID: 3606560

  • 21. Characterization of glucose-6-phosphate dehydrogenase variants. I. Occurrence of a G6PD Seattle-like variant in Sardinia and its interaction with the G6PD Mediterranean variant.
    Lenzerini L, Meera Khan P, Filippi G, Rattazzi MC, Ray AK, Siniscalco M.
    Am J Hum Genet; 1969 Mar; 21(2):142-53. PubMed ID: 5305539
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  • 26. Incidence and characteristics of glucose-6-phosphate dehydrogenase variants in Japan.
    Nakatsuji T, Miwa S.
    Hum Genet; 1979 Oct 02; 51(3):297-305. PubMed ID: 511159
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  • 30. Two distinct Indian G6PD variants G6PD Jamnagar and G6PD Rohini caused by the same 949 G-->A mutation.
    Sukumar S, Mukherjee MB, Colah RB, Mohanty D.
    Blood Cells Mol Dis; 2005 Oct 02; 35(2):193-5. PubMed ID: 15996881
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  • 33. [Characteristics of two new mutant forms of erythrocyte glucose-6-phosphate dehydrogenase: "Kirovograd" G6PD and "Zhitomir" G6PD].
    Shatskaia TL, Krasnopol'skaia KD, Idel'son LI.
    Genetika; 1976 Oct 02; 12(6):150-4. PubMed ID: 11150
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  • 34. Three major glucose-6-phosphate dehydrogenase-deficient polymorphic variants identified in Mazandaran state of Iran.
    Mesbah-Namin SA, Sanati MH, Mowjoodi A, Mason PJ, Vulliamy TJ, Noori-Daloii MR.
    Br J Haematol; 2002 Jun 02; 117(3):763-4. PubMed ID: 12028056
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  • 38. Detailed functional analysis of two clinical glucose-6-phosphate dehydrogenase (G6PD) variants, G6PDViangchan and G6PDViangchan+Mahidol: Decreased stability and catalytic efficiency contribute to the clinical phenotype.
    Boonyuen U, Chamchoy K, Swangsri T, Saralamba N, Day NP, Imwong M.
    Mol Genet Metab; 2016 Jun 02; 118(2):84-91. PubMed ID: 27053284
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  • 39. Two new glucose-6 phosphate dehydrogenase (G6PD) variants associated with hemolytic anemia: G6PD Amman-1 and G6PD Amman-2.
    Karadsheh NS, Awidi AS, Tarawneh MS.
    Am J Hematol; 1986 Jun 02; 22(2):185-92. PubMed ID: 3706292
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  • 40. Molecular analysis of G6PD variants in northern Italy: a study on the population from the Ferrara district.
    Ninfali P, Baronciani L, Ruzzo A, Fortini C, Amadori E, Dall'ara G, Magnani M, Beutler E.
    Hum Genet; 1993 Sep 02; 92(2):139-42. PubMed ID: 8370579
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