Beutler E: G6PD deficiency. Blood. 1994, 84: 3613-3636.
CAS
PubMed
Google Scholar
Cappellini MC, Fiorelli G: Glucose-6-phosphate dehydrogenase deficiency. Lancet. 2008, 371: 64-74. 10.1016/S0140-6736(08)60073-2.
Article
CAS
PubMed
Google Scholar
Mehta A, Mason PJ, Vulliamy TJ: Glucose-6-phosphate dehydrogenase deficiency. Bailliere Clinical Hematology. 2000, 13: 21-38.
Article
CAS
Google Scholar
Beutler E, Vulliamy TJ: Hematologically important mutations: glucose-6-phosphate dehydrogenase. Blood Cells Mol Dis. 2002, 28: 93-103. 10.1006/bcmd.2002.0490.
Article
PubMed
Google Scholar
Nakatsuji T, Miwa S: Incidence and characteristics of glucose-6-phosphate dehydrogenase variants in Japan. Hum Genet. 1979, 51: 297-305.
Article
CAS
PubMed
Google Scholar
Nikhoma ET, Poole C, Vannappagari V, Hall SA, Beutler E: The Global prevalence of glucose-6-phosphate dehydrogenase deficiency: A systemic review and meta-analysis. Blood Cells Mol Dis. 2009, 42: 267-278. 10.1016/j.bcmd.2008.12.005.
Article
Google Scholar
Oppenheim A, Lury CL, Rund D, Vulliamy TJ, Luzzatto L: G6PD Mediterranean accounts for the high prevalence of G6PD deficiency in Kurdish Jews. Hum Genet. 1993, 91: 293-294.
Article
CAS
PubMed
Google Scholar
Amin-Zaki L, Taj Al-Din S, Kubba K: Glucose-6-phosphate dehydrogenase deficiency among ethnic groups in Iraq. Bull World Health Organ. 1972, 47 (1): 1-5.
CAS
PubMed
PubMed Central
Google Scholar
Hamamy H, Saeed T: Glucose-6-phosphate dehydrogenase deficiency in Iraq. Hum Genet. 1981, 58: 434-435.
Article
CAS
PubMed
Google Scholar
Hilmi FA, Al-Allawi NA, Rassam M, Al-Shamma G, Al-Hashimi A: Red cell glucose-6-phosphate dehydrogenase phenotypes in Iraq. East Mediterr Health J. 2002, 8: 1-6.
Google Scholar
Hassan MK, Taha JY, Al-Naama LM, Widad NM, Jasim SN: Frequency of haemoglobinopathies and glucose-6-phosphate dehydrogenase deficiency in Basra. East Mediterr Health J. 2003, 9: 1-7.
Google Scholar
Al-Allawi N, Eissa AA, Jubrael JMS, Jamal SAR, Hamamy H: Prevalence and Molecular Characterization of Glucose-6-Phosphate Dehydrogenase Deficient Variants among the Kurdish population of Northern Iraq. BMC Blood Disorders. 2010, 10: 6-10.1186/1471-2326-10-6.
PubMed
PubMed Central
Google Scholar
Brewer GJ, Tarlove AR, Alving AS: The methemoglobin reduction test from primaquine-type sensitivity to erythrocytes. JAMA. 1962, 180: 386-388. 10.1001/jama.1962.03050180032008.
Article
CAS
PubMed
Google Scholar
Encyclopedia Britannica. [http://www.britannica.com/EBchecked/topic/293631/Iraq/214199/History]
Eissa AA, Muhammad FA, Mohammed AI, Al-Allawi NA, Jalal SD, Jubrael JMS: Prevalence and molecular characterization of G6PD deficient variants in Sulymania province-Iraq. Duhok Med J. 2011, 5: 69-75.
Google Scholar
White JM, Byrne M, Richards R, Buchanan T, Katsoulis E, Weerasingh K: Red cell genetic abnormalities in Peninsular Arabs: sickle haemoglobin, G6PD deficiency, and alpha and beta thalassaemia. J Med Genet. 1986, 23: 245-251. 10.1136/jmg.23.3.245.
Article
CAS
PubMed
PubMed Central
Google Scholar
Karadsheh NS, Moses L, Ismail SI, Devaney JM, Hoffman E: Molecular heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Jordan. Haematologica. 2005, 90: 1693-1694.
CAS
PubMed
Google Scholar
AlFadhli S, Kaaba S, Elshafey A, Salim M, AlAwadi A, Bastaki L: Molecular characterization of glucose-6-phosphate dehydrogenase gene defect in the Kuwaiti population. Arch Path Lab Med. 2005, 129: 1144-1147.
CAS
PubMed
Google Scholar
Al-Ali AK, Al-Mustafa ZH, Al-Madan M, Qaw F, Al-Ateeq S: Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the eastern Province of Saudi Arabia. Clin Chem Lab Med. 2002, 40: 814-816.
Article
CAS
PubMed
Google Scholar
Bayoumi RA, Nur-E-Kamal MS, Tadayyon M, Mohamed KK, Mahboob BH, Qureshi MM, Lakhani MS, Awaad MO, Kaeda J, Vulliamy TJ, Luzzatto L: Molecular characterization of erythrocyte glucose-6-phosphate dehydrogenase deficiency in Al-Ain District, United Arab Emirates. Hum Hered. 1996, 46: 136-141. 10.1159/000154342.
Article
CAS
PubMed
Google Scholar
Arnaout NH, El-Gharbawy NM, Shaheen IA, Afifi RA, Abd El-Dayem OY: Incidence and Association of 563 C/T Mediterranean and the Silent 1311 C/T mutations in G6PD-deficient Egyptian Children. LabMedicine. 2011, 42: 355-360.
Google Scholar
Al-Momen N, Al Arrayed SS, Al Allawi A: Molecular homogeneity of GPD Deficiency. Bahrain Medical Bulletin. 2004, 26: 1-6.
Google Scholar
Nafa K, Reghis A, Osmani N, Baghli L, Ait-Abbes H, Benabadji M, Kaplan J-C, Vulliamy T, Luzzatto L: At least five polymorphic variants account for the prevalence of glucose 6-phosphate deficiency in Algeria. Hum Genet. 1994, 94: 513-517.
Article
CAS
PubMed
Google Scholar
Ben Daoud B, Mosbehi I, Prehu C, Chaouachi D, Hafsia R, Abbes S: Molecular characterization of erythrocyte glucose-6-phosphate dehydrogenase deficiency in Tunisia. Pathol Biol. 2008, 56: 260-267. 10.1016/j.patbio.2007.08.009.
Article
PubMed
Google Scholar
Oner R, Gumruk F, Acar C, Oner C, Gurgey A, Altay C: Molecular characterization of glucose-6- phosphate dehydrogenase deficiency in Turkey. Haematologica. 2000, 85: 320-321.
CAS
PubMed
Google Scholar
Mesbah-Namin SA, Sanati MH, Momjoodi AR, Mason PJ, Vullamy TJ, Noori-Daloii MR: Three major glucose-6-phosphate dehydrogenase deficient polymorphic variants identified in Mazandaran state of Iran. Brit J Haematol. 2002, 117: 763-764. 10.1046/j.1365-2141.2002.03483.x.
Article
CAS
Google Scholar
Rahimi Z, Vaisi-Raygani A, Nagel RL, Muniz A: Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Kurdish population of Western Iran. Blood Cells Mol Dis. 2006, 37: 31-37.
Article
Google Scholar
Karimi M, Martinez Di Montemuros F, Danielli MG, Farjadian S, Afrasiabi A, Fiorelli G, Cappellini MD: Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Fars province of Iran. Haematologica. 2003, 88: 346-347.
PubMed
Google Scholar
Sukumar S, Mukherjee MB, Colah RB, Mohanty D: Molecular basis of G6PD deficiency in India. Blood cell Mol Dis. 2004, 33: 141-145. 10.1016/j.bcmd.2004.06.003.
Article
CAS
Google Scholar
Moiz B, Nasir A, Moatter T, Naqvi ZA, Khurshid M: Population study of 1311 C/T polymorphism of glucose 6 phosphate dehydrogenase gene in Pakistan - an analysis of 715 X-chromosomes. BMC Genet. 2009, 10: 41-
Article
PubMed
PubMed Central
Google Scholar
Martinez Di Montemuros F, Dotti C, Tavazzi D, Fiorelli G, Cappellini MD: Molecular heterogeneity of glucose-6-phosphate dehydrogenase (G6PD) variants in Italy. Haematologica. 1997, 82: 440-445.
CAS
PubMed
Google Scholar
Menounos P, Zervas C, Garinis G, Doukas C, Kolokithopoulos D, Tegos C, Patrinos GP: Molecular heterogeneity of the glucose-6-phosphate dehydrogenase deficiency in the Hellenic population. Hum Hered. 2000, 50: 237-241. 10.1159/000022922.
Article
CAS
PubMed
Google Scholar
Ainoon O, Yu YH, Amir Muhriz AL, Boo NY, Cheong SK, Hamidah NH: Glucose-6-phosphate dehydrogenase (G6PD) variants in Malaysian Malays. Hum Mutat. 2003, 21: 101-
Article
CAS
PubMed
Google Scholar
Soemantri AG, Saha S, Saha N, Tay JSH: Molecular variants of red cell glucose-6-phosphate dehdrogenase deficiency in central Java, Indonesia. Hum Hered. 1995, 45: 346-350. 10.1159/000154303.
Article
CAS
PubMed
Google Scholar
Kurdi-Haidar B, Mason PJ, Berrebi A, Ankra-Badu G, Al-Ali A, Oppenhheim A, Luzzatto L: Origin and spread of glucose-6-phosphate dehydrogenase variant (G6PD-Mediterranean) in the Middle East. Am J Hum Genet. 1990, 47: 1013-1019.
CAS
PubMed
PubMed Central
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. 1990, 47: 1008-1012.
CAS
PubMed
PubMed Central
Google Scholar
Tishkoff SA, Vasrkonyi R, Cahinhinan N, Abbes S, Argyropoulos G, Destro-Bisol G, Drousiotou A, Dangerfield B, Lefranc G, Loiselet J, Piro A, Stoneking M, Tagarelli A, Tagarelli G, Touma EH, Williams SM, Clark AG: Haplotype diversity and Linkage disequilibrium at human G6PD: Recent origin of alleles that confer malarial resistance. Science. 2001, 293: 455-462. 10.1126/science.1061573.
Article
CAS
PubMed
Google Scholar
Vives Corrons JL, Zarza R, Aymerich JM, Boixadera J, Carrera A, Colomer D, Corbella M, Castro M, Crespo JM, Del Arco A, Erkiaga S, Font L, González I, Juncá J, Lausin A, Manrubia E, Martin Núňez G, Murga MJ, Oliva E, Pérez De Mendiguren B, Pujades MA, Remacha A, Rovira A, Villegas A: Molecular analysis of glucose-6-dehydrogenase deficiency in Spain. Sangre (Barc). 1997, 42: 391-398.
CAS
Google Scholar
Kawamoto F, Matsuoka H, Kanbe T, Tantular IS, Pusarauati S, Kerong HI, Damianus W, Mere D, Dachlan YP: Further investigations of glucose-6-phosphate dehydrogenase variations in Flores Island, eastern Indonesia. J Hum Genet. 2006, 51: 952-957. 10.1007/s10038-006-0044-y.
Article
CAS
PubMed
Google Scholar
Nafa K, Reghis A, Osmani N, Baghli L, Benabadji M, Kaplan JC, Vulliamy TJ, Luzzatto L: G6PD Aures: a new mutation (48 Ile- > Thr) causing mild G6PD deficiency is associated with favism. Hum Mol Genet. 1993, 2: 81-82. 10.1093/hmg/2.1.81.
Article
CAS
PubMed
Google Scholar
Al Jaouni SK: Molecular clinical correlation of glucose 6-phosphate deficiency in western Saudi Arabia. Haematologica. 2006, 91 (S1): 24-25.
Google Scholar
Al-Ali AK: Common G6PD variant from Saudi population and its prevalence. Ann Saudi Med. 1996, 16: 654-656.
CAS
PubMed
Google Scholar
Al Arrayed S: Campaign to control genetic blood diseases in Bahrain. Community Genet. 2005, 8: 52-55. 10.1159/000083340.
Article
CAS
PubMed
Google Scholar
Usanga EA, Ameen R: Glucose-6-phosphate dehydrogenase deficiency in Kuwait, Syria, Egypt, Iran, Jordan and Lebanon. Hum Hered. 2000, 50: 158-161. 10.1159/000022906.
Article
CAS
PubMed
Google Scholar
El Fakhri M: Glucose-6-phosphate dehydrogenase deficiency in Libya: an appraisal of gene frequency in Arabic regions of Africa and West Asia. Garyounis Med J. 1985, 8: 143-146.
Google Scholar
Al-Riyami A, Ebrahim GJ: Genetic Blood Disorders Survey in the Sultanate of Oman. J Trop Pediatr. 2003, 49 (Suppl 1): i1-i20.
PubMed
Google Scholar
Alabdulaali MK, Alayed KM, Alshaikh AF, Almashhadani SA: Prevalence of glucose-6-phosphate dehydrogenase deficinecy and sickle cell trait among blood donors in Riyadh. Asian J Transf Sci. 2010, 4: 31-33. 10.4103/0973-6247.59389.
Article
CAS
Google Scholar
Warsy AS, El-Hazmi MAF: G6PD deficiency, distribution and variants in Saudi Arabia: an overview. Ann Saudi Med. 2001, 21: 174-177.
CAS
PubMed
Google Scholar
Omer A, Ali M, Omer AH, Mustafa MD, Satir AA, Samuel AP: Incidence of G-6-PD deficiency and abnormal haemoglobins in the indigenous and immigrant tribes of the Sudan. Trop Geogr Med. 1972, 24: 401-405.
CAS
PubMed
Google Scholar
Altay C, Gümrük F: Red Cell glucose-6-phosphate dehydrogenase deficiency in Turkey. Turk J Hematol. 2008, 25: 1-7.
CAS
Google Scholar
Clark TG, Fry AE, Auburn S, Campino S, Diakite M, Green A, Richardson A, Teo YY, Small K, Wilson J, Jallow M, Sisay-Joof F, Pinder M, Sabeti P, Kwiatkowski DP, Rockett KA: Allelic heterogeneity of G6PD deficiency in West Africa and severe malaria susceptibility. Eur J Hum Genet. 2009, 17: 1080-1085. 10.1038/ejhg.2009.8.
Article
CAS
PubMed
PubMed Central
Google Scholar
Bouanga JC, Mouélé R, Préhu C, Wajcman H, Feingold J, Galactéros F: Glucose-6-phosphate dehydrogenase deficiency and homozygous sickle cell disease in Congo. Hum Hered. 1998, 48: 192-197.
Article
CAS
PubMed
Google Scholar
Carter N, Pamba A, Duparc S, Waitumbi JN: Frequency of glucose-6-phosphate dehydrogenase deficiency in malaria patients from six African countries enrolled in two randomized anti-malarial clinical trials. Malaria J. 2011, 10: 241-10.1186/1475-2875-10-241.
Article
CAS
Google Scholar
Khneisser I, Adib SM, Loiselet J, Megarbane A: Prevalence of G6PD deficiency and knowledge of diagnosis in a sample of previously unscreened Lebanese males: clinical implications. J Med Screen. 2006, 13: 26-28. 10.1258/096914106776179827.
Article
PubMed
Google Scholar
Luzzatto L, Notaro R: Malaria. Protection against bad air. Science. 2001, 293: 442-443. 10.1126/science.1063292.
Article
CAS
PubMed
Google Scholar
Morsy H, Mokhtar M, Nazmy N, El-Gezeery A, Abdulla E: Neonatal screening and molecular genetic characterization of glucose-6-phosphate dehydrogenase deficiency in Alexandria, Egypt. HUGO J. 2011, 5: 229-
Google Scholar