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24. 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 [TBL] [Abstract][Full Text] [Related]
25. [The C1155G mutation of the red blood cell glucose-6-phosphate dehydrogenase gene in a subject with severe hereditary chronic nonspherocytic anaemia]. Burzyńska B; Adamowicz-Salach A; Płochocka D; Gołaszewska E; Witos I Med Wieku Rozwoj; 2009; 13(2):136-9. PubMed ID: 19837994 [TBL] [Abstract][Full Text] [Related]
26. Hemolysis and Mediterranean G6PD mutation (c.563 C>T) and c.1311 C>T polymorphism among Palestinians at Gaza Strip. Sirdah M; Reading NS; Perkins SL; Shubair M; Aboud L; Prchal JT Blood Cells Mol Dis; 2012 Apr; 48(4):203-8. PubMed ID: 22364808 [TBL] [Abstract][Full Text] [Related]
27. Definition of the mutations of G6PD Wayne, G6PD Viangchan, G6PD Jammu, and G6PD 'LeJeune'. Beutler E; Westwood B; Kuhl W Acta Haematol; 1991; 86(4):179-82. PubMed ID: 1805484 [TBL] [Abstract][Full Text] [Related]
28. A new glucose-6-phosphate dehydrogenase variant with congenital nonspherocytic hemolytic anemia (G6PD Genova). Biochemical characterization and mosaicism expression in the heterozygote. Gaetani GF; Galiano S; Melani C; Miglino M; Forni GL; Napoli G; Perrone L; Ferraris AM Hum Genet; 1990 Mar; 84(4):337-40. PubMed ID: 2307454 [TBL] [Abstract][Full Text] [Related]
29. Possible association of 3' UTR +357 A>G, IVS11-nt 93 T>C, c.1311 C>T polymorphism with G6PD deficiency. Sirdah MM; Shubair ME; Al-Kahlout MS; Al-Tayeb JM; Prchal JT; Reading NS Hematology; 2017 Jul; 22(6):370-374. PubMed ID: 28059001 [TBL] [Abstract][Full Text] [Related]
30. Distinct phenotypic expression of two de novo missense mutations affecting the dimer interface of glucose-6-phosphate dehydrogenase. van Wijk R; Huizinga EG; Prins I; Kors A; Rijksen G; Bierings M; van Solinge WW Blood Cells Mol Dis; 2004; 32(1):112-7. PubMed ID: 14757424 [TBL] [Abstract][Full Text] [Related]
32. Three new exon 10 glucose-6-phosphate dehydrogenase mutations. Beutler E; Westwood B; Melemed A; Dal Borgo P; Margolis D Blood Cells Mol Dis; 1995; 21(1):64-72. PubMed ID: 7655862 [TBL] [Abstract][Full Text] [Related]
33. Glucose-6 phosphate dehydrogenase mutations and haplotypes in various ethnic groups. Xu W; Westwood B; Bartsocas CS; Malcorra-Azpiazu JJ; Indrák K; Beutler E Blood; 1995 Jan; 85(1):257-63. PubMed ID: 7803800 [TBL] [Abstract][Full Text] [Related]
34. Identification of a single base change in a new human mutant glucose-6-phosphate dehydrogenase gene by polymerase-chain-reaction amplification of the entire coding region from genomic DNA. Poggi V; Town M; Foulkes NS; Luzzatto L Biochem J; 1990 Oct; 271(1):157-60. PubMed ID: 2222408 [TBL] [Abstract][Full Text] [Related]
35. Molecular analysis of eight biochemically unique glucose-6-phosphate dehydrogenase variants found in Japan. Hirono A; Fujii H; Takano T; Chiba Y; Azuno Y; Miwa S Blood; 1997 Jun; 89(12):4624-7. PubMed ID: 9192788 [TBL] [Abstract][Full Text] [Related]
36. Neonatal jaundice and molecular mutations in glucose-6-phosphate dehydrogenase deficient newborn infants. Huang CS; Hung KL; Huang MJ; Li YC; Liu TH; Tang TK Am J Hematol; 1996 Jan; 51(1):19-25. PubMed ID: 8571933 [TBL] [Abstract][Full Text] [Related]
37. Mutation analysis of glucose-6-phosphate dehydrogenase (G6PD) variants in Costa Rica. Beutler E; Kuhl W; Sáenz GF; Rodríguez W Hum Genet; 1991 Aug; 87(4):462-4. PubMed ID: 1879833 [TBL] [Abstract][Full Text] [Related]
38. Marked decrease in specific activity contributes to disease phenotype in two human glucose 6-phosphate dehydrogenase mutants, G6PD(Union) and G6PD(Andalus). Wang XT; Lam VM; Engel PC Hum Mutat; 2005 Sep; 26(3):284. PubMed ID: 16088936 [TBL] [Abstract][Full Text] [Related]
39. Chronic nonspherocytic hemolytic anemia (CNSHA) and glucose 6 phosphate dehydrogenase (G6PD) deficiency in a patient with familial amyloidotic polyneuropathy (FAP). Molecular study of a new variant (G6PD Clinic) with markedly acidic pH optimum. Vives-Corrons JL; Pujades MA; Petit J; Colomer D; Corbella M; Aguilar i Bascompte JL; Merino A Hum Genet; 1989 Jan; 81(2):161-4. PubMed ID: 2912886 [TBL] [Abstract][Full Text] [Related]
40. Characterization of G6PD deficiency in southern Croatia: description of a new variant, G6PD Split. Barišić M; Korać J; Pavlinac I; Krželj V; Marušić E; Vulliamy T; Terzić J J Hum Genet; 2005; 50(11):547-549. PubMed ID: 16143877 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]