P. J. Mason, J. M. Bautista, and F. Gilsanz, G6PD deficiency: the genotype-phenotype association, Blood Reviews, vol.21, issue.5, pp.267-283, 2007.
DOI : 10.1016/j.blre.2007.05.002

A. Drousiotou, E. H. Touma, N. Andreou, J. Loiselet, M. Angastiniotis et al., Molecular characterization of G6PD deficiency in Cyprus, Blood Cells, Molecules, and Diseases, vol.33, issue.1, pp.33-58, 2004.
DOI : 10.1016/j.bcmd.2004.03.004

A. Minucci, K. Moradkhani, M. J. Hwang, C. Zuppi, B. Giardina et al., Glu- cose-6-phosphate dehydrogenase (G6PD) mutations database: review of the " old " and update of the new mutations, Blood Cells Mol. Dis, pp.48-154, 2012.

B. Kurdi-haidar, P. J. Mason, A. Berrebi, G. Ankra-badu, A. Ali et al., Origin and spread of the glucose-6-phosphate dehydrogenase variant (G6PD-Mediterranean) in the Middle East, Am. J. Hum. Genet, pp.47-1013, 1990.

H. Wen, Y. Li, C. Qi, Y. Jiang, C. Zheng et al., Structure and function of glucose-6-phosphate dehydrogenase-deficient variants in Chinese population, Hum. Genet, vol.119, pp.463-478, 2006.

B. B. Daoud, I. Mosbehi, C. Préhu, D. Chaouachi, R. Hafsia et al., Molecular characterization of erythrocyte glucose-6-phosphate dehydrogenase deficiency in Tunisia, Pathologie Biologie, vol.56, issue.5, pp.56-260, 2008.
DOI : 10.1016/j.patbio.2007.08.009
URL : https://hal.archives-ouvertes.fr/pasteur-01375220

N. Guellouz, I. B. Mansour, M. Ouederni, S. Jabnoun, S. Kacem et al., Neonatal screening of G6PD deficiency in Tunisia, Arch. Inst. Pasteur Tunis, vol.87, pp.69-76, 2010.

A. Hirono and E. Beutler, Molecular cloning and nucleotide sequence of cDNA for human glucose-6-phosphate dehydrogenase variant A(-)., Proceedings of the National Academy of Sciences, vol.85, issue.11, pp.85-3951, 1988.
DOI : 10.1073/pnas.85.11.3951

T. J. Vulliamy, M. D. Urso, G. Battistuzzi, M. Estrada, N. S. Foulkes et al., Diverse point mutations in the human glucose-6-phosphate dehydrogenase gene cause enzyme deficiency and mild or severe hemolytic anemia., Proceedings of the National Academy of Sciences, vol.85, issue.14, pp.5171-5175, 1988.
DOI : 10.1073/pnas.85.14.5171

Y. Okano, A. Fujimoto, T. Miyagi, A. Hirono, S. Miwa et al., Two novel glucose-6-phosphate dehydrogenase variants found in newborn mass-screening for galactosaemia, European Journal of Pediatrics, vol.160, issue.2, pp.160-105, 2001.
DOI : 10.1007/s004310000652

L. Luzzatto, Glucose-6-Phosphate Dehydrogenase Deficiency, Hematology/Oncology Clinics of North America, vol.30, issue.2, pp.1303-1306, 2006.
DOI : 10.1016/j.hoc.2015.11.006

P. Rowland, A. K. Basak, S. Gover, H. R. Levy, and M. J. Adams, The three???dimensional structure of glucose 6???phosphate dehydrogenase from Leuconostoc mesenteroides refined at 2.0 ?? resolution, Structure, vol.2, issue.11, pp.1073-1087, 1994.
DOI : 10.1016/S0969-2126(94)00110-3

S. W. Au, S. Gover, V. M. Lam, and M. J. Adams, Human glucose-6-phosphate dehydrogenase: the crystal structure reveals a structural NADP+ molecule and provides insights into enzyme deficiency, Structure, vol.8, issue.3, pp.293-303, 2000.
DOI : 10.1016/S0969-2126(00)00104-0

T. Takizawa, Y. Yoneyama, S. Miwa, and A. Yoshida, A single nucleotide base transition is the basis of the common human glucose-6-phosphate dehydrogenase variant A(+), Genomics, vol.1, issue.3, pp.228-231, 1987.
DOI : 10.1016/0888-7543(87)90048-6

A. Hirono, K. Kawate, A. Honda, H. Fujii, and S. Miwa, A single mutation 202G>A in the human glucose-6-phosphate dehydrogenase gene (G6PD) can cause acute hemolysis by itself, Blood, vol.99, issue.4, p.1498, 2002.
DOI : 10.1182/blood.V99.4.1498

M. D. Cappellini, M. Sampietro, D. Toniolo, G. Carandina, F. Martinez-di-montemuros et al., G6PD Ferrara I has the same two mutations as G6PD A(-) but a distinct biochemical phenotype, Human Genetics, vol.93, issue.2, pp.93-139, 1994.
DOI : 10.1007/BF00210598

E. Beutler, B. Westwood, J. T. Prchal, G. Vaca, C. S. Bartsocas et al., New glucose-6-phosphate dehydrogenase mutations from various ethnic groups, Blood, vol.80, pp.255-256, 1992.

E. Beutler, W. Kuhl, J. L. Vives-corrons, and J. T. Prchal, Molecular heterogeneity of glucose-6-phosphate dehydrogenase A?, Blood, vol.74, pp.2550-2555, 1989.

T. Vulliamy, A. Rovira, N. Yusoff, D. Colomer, L. Luzzatto et al., Independent origin of single and double mutations in the human glucose 6-phosphate dehydrogenase gene, Human Mutation, vol.85, issue.4, pp.311-318, 1996.
DOI : 10.1002/(SICI)1098-1004(1996)8:4<311::AID-HUMU3>3.0.CO;2-A

E. Beutler, W. Kuhl, G. F. Sáenz, and W. Rodríguez, Mutation analysis of glucose-6-phosphate dehydrogenase (G6PD) variants in Costa Rica, Human Genetics, vol.87, issue.4, pp.462-464, 1991.
DOI : 10.1007/BF00197169

E. Beutler, W. Kuhl, T. Gelbart, and L. Forman, DNA sequence abnormalities of human glucose-6-phosphate dehydrogenase variants, J. Biol. Chem, vol.266, pp.4145-4150, 1991.

A. R. Hamel, I. R. Cabral, T. S. Sales, F. F. Costa, and S. T. Saad, Molecular Heterogeneity of G6PD Deficiency in an Amazonian Population and Description of Four New Variants, Blood Cells, Molecules, and Diseases, vol.28, issue.3, pp.399-406, 2002.
DOI : 10.1006/bcmd.2002.0524

G. Vaca, B. Ibarra, F. Romero, N. Olivares, J. M. Cantú et al., A new mutant associated with chronic nonspherocytic hemolytic anemia, Hum. Genet, pp.61-175, 1982.

A. Vlachos, B. Westwood, J. M. Lipton, and E. Beutler, G6PD Mount Sinai: A new severe hemolytic variant characterized by dual mutations at nucleotides 376G and 1159T (N126D), Human Mutation, vol.45, issue.S1, pp.154-155, 1998.
DOI : 10.1002/humu.1380110151

P. Menounos, C. Zervas, G. Garinis, C. Doukas, D. Kolokithopoulos et al., Molecular Heterogeneity of the Glucose-6-Phosphate Dehydrogenase Deficiency in the Hellenic Population, Human Heredity, vol.50, issue.4, pp.50-237, 2000.
DOI : 10.1159/000022922

Z. Yang, J. Chu, G. Ban, X. Huang, S. Xu et al., The genotype analysis of glucose-6- phosphate dehydrogenase deficiency in Yunnan province, Zhonghua Yi Xue Yi Chuan Xue Za Zhi, vol.18, pp.259-263, 2001.