References
- Mohandas N., Clark M. R., Jacobs M. S., Shohet S. B. Analysis of factors regulating erythrocyte deformability. J Clin Invest 1980; 66: 563–73
- Mehta A., Mason P. J., Vulliamy T. J. Glucose‐6‐phosphate dehydrogenase deficiency. Baillières Best Pract Res Clin Haematol 2000; 13: 21–38
- Pandolfi P. P., Sonati F., Rivi R., Mason P., Grosveld F., Luzzatto L. Targeted disruption of the housekeeping gene encoding glucose 6‐phosphate dehydrogenase (G6PD): G6PD is dispensable for pentose synthesis but essential for defense against oxidative stress. Embo J 1995; 14: 5209–15
- Dern R. J., Weinstein I. M., Leroy G. V., Talmage D. W., Alving A. S. The hemolytic effect of primaquine. I. The localization of the drug‐induced hemolytic defect in primaquine‐sensitive individuals. J Lab Clin Med 1954; 43: 303–9
- Carson P. E., Flanagan C. L. Enzymatic deficiency in primaquine‐sensitive erythrocytes. Science 1956; 124: 484–9
- Beutler E. G6PD deficiency. Blood 1994; 84: 3613–36
- Yoshida A. Glucose 6‐phosphate dehydrogenase of human erythrocytes. I. Purification and characterization of normal (B+) enzyme. J Biol Chem 1966; 241: 4966–76
- Takizawa T., Huang I. Y., Ikuta T., Yoshida A. Human glucose‐6‐phosphate dehydrogenase: primary structure and cDNA cloning. Proc Natl Acad Sci USA 1986; 83: 4157–61
- Martini G., Toniolo D., Vulliamy T., Luzzatto L., Dono R., Viglietto G., et al. Structural analysis of the X‐linked gene encoding human glucose 6‐phosphate dehydrogenase. Embo J 1986; 5: 1849–55
- Persico M. G., Viglietto G., Martini G., Toniolo D., Paonessa G., Moscatelli C., et al. Isolation of human glucose‐6‐phosphate dehydrogenase (G6PD) cDNA clones: primary structure of the protein and unusual 5' non‐coding region. Nucl Acids Res 1986; 14: 2511–22
- Filosa S., Calabro V., Lania G., Vulliamy T. J., Brancati C., Tagarelli A., et al. G6PD haplotypes spanning Xq28 from F8C to red/green color vision. Genomics 1993; 17: 6–14
- Beutler E., Vulliamy T., Luzzatto L. Hematologically important mutations: glucose‐6‐phosphate dehydrogenase. Blood Cells Mol Dis 1996; 22: 49–56
- Siniscalco M., Filippi G., Latte B. Recombination between protan and deutan genes; data on their relative positions in respect of the G6pd locus. Nature 1964; 204: 1062–4
- Piomelli S., Corash L. M., Davenport D. D., Miraglia J., Amorosi E. L. In vivo lability of glucose‐6‐phosphate dehydrogenase in GdA‐ and Gd‐Mediterranean deficiency. J Clin Invest 1968; 47: 940–8
- Morelli A., Benatti U., Gaetani G. F., De Flora A. Biochemical mechanisms of glucose‐6‐phosphate dehydrogenase deficiency. Proc Natl Acad Sci USA 1978; 75: 1979–83
- Kaplan M., Hammerman C. Glucose‐6‐phosphate dehydrogenase‐deficient neonates: a potential cause for concern in North America. Pediatrics 2000; 106: 1478–9
- Valaes T. Severe neonatal jaundice associated with glucose‐6‐phosphate dehydrogenase deficiency: pathogenesis and global epidemiology. Acta Paediatr 1994; Suppl 394: 58–76
- Tan K. L. Glucose‐6‐phosphate dehydrogenase status and neonatal jaundice. Arch Dis Child 1981; 56: 874–7
- Ruwende C., Hill A. Glucose‐6‐phosphate dehydrogenase deficiency and malaria. J Mol Med 1998; 76: 581–8
- Frank J. E. Diagnosis and management of G6PD deficiency. Am Fam Phys 2005; 72: 1277–82
- Beutler E. Hemolytic anemia in disorders of red cell metabolism 1978, New York. Plenum Press