Restriction fragment length polymorphism (RFLP) of the X chromosome linked glucose-6-phosphate dehydrogenase (G6PD) locus in India

References

• Beutler E. 1992. The molecular biology of G6PD variants and other red cell enzyme defects. Ann Rev Med. 43:47–59.
   PubMedGoogle Scholar
• Beutler E. 1993. Study of glucose-6-phosphate dehydrogenase: History and Molecular Biology. Am J Hematol. 42:53–58.
   PubMedGoogle Scholar
• Beutler E. 1994. G6PD deficiency. Blood. 84:3613–3636.
   PubMed Web of Science ®Google Scholar
• Beutler E, Kuhl W. The NT 1311 polymorphism of G6PD: G6PD Mediterranean mutation may have originated independently in Europe and Asia. Am J Hum Genet. 1990a; 47:1008–1012.
   PubMed Web of Science ®Google Scholar
• Beutler E, Kuhl W. Linkage between a PvuII restriction fragment length polymorphism and G6PD A-202A/376G: Evidence for a single origin of the common G6PD A − mutation. Hum Genet. 1990b; 85:9–11.
   PubMedGoogle Scholar
• Beutler E, Kuhl W, Vives-Corrons JL, Prchal JT. 1989. Molecular heterogeneity of glucose-6-phosphate dehydrogenase A − . Blood. 74:2550–2555.
   PubMed Web of Science ®Google Scholar
• Cann RL. 2001. Genetic clues to dispersal of human populations: Retracing the past from the present. Science. 291:1742–1748.
   PubMed Web of Science ®Google Scholar
• Cappellini MD, Fiorelli G. 2008. Glucose-6-phosphate dehydrogenase deficiency. Lancet. 371:64–74.
   PubMed Web of Science ®Google Scholar
• Chalvam R, Colah RB, Mohanty D, Ghosh K, Mukherjee MB. 2009. Molecular heterogeneity of glucose-6-phosphate dehydrogenase deficiency among the tribals in Western India. Blood Cells Mol Dis. 43:156–157.
   PubMedGoogle Scholar
• Chalvam R, Kedar PS, Colah RB, Ghosh K, Mukherjee MB. 2008. A novel R198H mutation in the glucose-6-phosphate dehydrogenase gene in the tribal groups of the Nilgiris in Southern India. J Hum Genet. 53:181–184.
   PubMedGoogle Scholar
• Chalvam R, Mukherjee MB, Colah RB, Mohanty D, Ghosh K. 2007. G6PD Namoru (208 T → C) is the major polymorphic variant in the tribal populations in southern India. Br J Haematol. 136:512–513.
   PubMedGoogle Scholar
• Excoffier L, Laval G, Schneider S. 2005. Arlequin ver.3.0: An integrated software package for population genetics data analysis. Evol Bioinform. 1:47–50.
   PubMed Web of Science ®Google Scholar
• Ganczakowski M, Town M, Bowden DK, Vulliamy TJ, Kaneko A, Clegg JB, Weatherall DJ, Luzzatto L. 1995. Multiple Glucose-6-Phosphate dehydrogenase deficient variants correlate with malaria endemicity in the Vanuatu Archipelago (South western Pacific). Am J Hum Genet. 56:294–301.
   PubMedGoogle Scholar
• Kaeda JS, Chhotray GP, Ranjit MR, Bautista JM, Reddy PH, Steven SD, Naidu JM, Britt RB, Vulliamy TJ, Luzzatto L, Mason PJ. 1995. A new glucose-6-phosphate dehydrogenase variant, G6PD Orissa (44Ala → Gly) is the major polymorphic variant in tribal population of India. Am J Hum Genet. 57:1335–1341.
   PubMedGoogle Scholar
• Kay CA, Kuhl W, Prchal J, Beutler E. 1992. The origin of glucose-6-phosphate dehydrogenase (G6PD) polymorphisms in African-Americans. Am J Hum Genet. 50:394–398.
   PubMedGoogle Scholar
• Majumder PP. 2001. Ethnic populations of India as seen from an evolutionary perspective. J Biosci. 26:533–545.
   PubMed Web of Science ®Google Scholar
• Manco L, Botigue LR, Ribeiro LM, Abade A. G6PD deficient alleles and haplotype analysis of human G6PD locus in Sao Tome e Principe (West Africa). Hum Biol. 2007a; 79:679–686.
   PubMedGoogle Scholar
• Manco L, Gonsalves P, Antunes P, Maduro F, Abade A, Ribeiro LM. Mutations and haplotype diversity in 70 Portuguese G6PD deficient individuals: An overview on the origin and evolution of mutated alleles. Haematologica. 2007b; 92:1713–1714.
   PubMed Web of Science ®Google Scholar
• McKusick VA. 1986. The human gene map. Cold Spring Harb Symp. Quant Biol. 51:1123–1208.
   PubMedGoogle Scholar
• Pietrapertosa A, Palma A, Campanale D, Delios G, Vitucci A, Tannoia N. 2001. Genotype and phenotype correlation in glucose-6-phosphate dehydrogenase deficiency. Haematologica. 86:30–35.
   PubMedGoogle Scholar
• Rodrigues MO, Friere AP, Martins MC, Monteiro C. 2002. Glucose-6-Phosphate dehydrogenase defifciency in Portugal: Biochemical and mutational profiles, heterogeneity and haplotype association. Blood Cells Mol Dis. 28:249–259.
   PubMed Web of Science ®Google Scholar
• Saad ST, Costa FF. 2003. Mild hemolysis in a girl with G6PD Sumaré (class I variant) associated with G6PD A − . Blood Cells Mol Dis. 30:238–240.
   PubMedGoogle Scholar
• Sukumar S, Mukherjee MB, Colah RB, Mohanty D. 2004. Molecular basis of G6PD deficiency in India. Blood cells Mol Dis. 33:141–145.
   PubMed Web of Science ®Google Scholar
• Vulliamy TJ, Othman A, Town M, Nathwani A, Falusi Y, Luzzatto L. Linkage disequilibrium of polymorphic sites in the G6PD gene in African populations and the origin of G6PD A − . Gene Geogr. 1991a; 5:13–21.
   PubMedGoogle Scholar
• Vulliamy TJ, Othman A, Town M, Nathwani A, Falusia AG, Mason PJ, Luzzatto L. Polymorphic sites in the African population detected by sequence analysis of G6PD gene outline the evolution of the variants A & A − . Proc Natl Acad Sci USA. 1991b; 88:8568–8571.
   PubMed Web of Science ®Google Scholar
• Yan T, Cai R, Mo OH, Zhu DL, Ouyang H, Huang L, Zhao M, Huang F, Li L, Liang X, Xu X. 2006. Incidence and complete molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Guangxi Zhuang autonomous region of southern China: Description of four novel mutations. Haematologica. 91:1321–1328.
   PubMed Web of Science ®Google Scholar