{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,9,24]],"date-time":"2023-09-24T10:28:27Z","timestamp":1695551307730},"reference-count":26,"publisher":"Springer Science and Business Media LLC","issue":"2","license":[{"start":{"date-parts":[[2012,10,14]],"date-time":"2012-10-14T00:00:00Z","timestamp":1350172800000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Mol Biol Rep"],"published-print":{"date-parts":[[2013,2]]},"DOI":"10.1007\/s11033-012-2124-8","type":"journal-article","created":{"date-parts":[[2012,10,17]],"date-time":"2012-10-17T18:33:31Z","timestamp":1350498811000},"page":"851-856","source":"Crossref","is-referenced-by-count":9,"title":["Glucose-6-phosphate dehydrogenase deficiency in Tunisia: molecular data and phenotype-genotype association"],"prefix":"10.1007","volume":"40","author":[{"given":"N.","family":"Laouini","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A.","family":"Bibi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"H.","family":"Ammar","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"K.","family":"Kazdaghli","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"F.","family":"Ouali","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"R.","family":"Othmani","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"S.","family":"Amdouni","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"S.","family":"Haloui","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C. A.","family":"Sahli","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"L.","family":"Jouini","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"S.","family":"Hadj Fredj","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"H.","family":"Siala","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"N.","family":"Ben Romdhane","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"N. E.","family":"Toumi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"S.","family":"Fattoum","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"T.","family":"Messsaoud","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2012,10,14]]},"reference":[{"key":"2124_CR1","first-page":"167","volume":"46","author":"N Daloii","year":"2008","unstructured":"Daloii N, Daneshpajooh M (2008) Molecular basis of G6PD deficiency: current status and its perspective. Acta Med Iran 46:167\u2013182","journal-title":"Acta Med Iran"},{"key":"2124_CR2","doi-asserted-by":"crossref","first-page":"246","DOI":"10.1038\/376246a0","volume":"376","author":"C Ruwende","year":"1995","unstructured":"Ruwende C, Khoo S, Snow R et al (1995) Natural selection of hemi- and heterozygotes for G6PD deficiency in Africa by resistance to severe malaria. Nature 376:246\u2013249","journal-title":"Nature"},{"key":"2124_CR3","doi-asserted-by":"crossref","first-page":"711","DOI":"10.1016\/j.crvi.2004.07.010","volume":"327","author":"H Wajcman","year":"2004","unstructured":"Wajcman H, Galact\u00e9ros F (2004) Le deficit en glucose-6-phosphate d\u00e9shydrog\u00e9nase: protection contre le paludisme et risque d\u2019accidents h\u00e9molytiques. C R Biol 327:711\u2013720","journal-title":"C R Biol"},{"key":"2124_CR4","doi-asserted-by":"crossref","first-page":"21","DOI":"10.1053\/beha.1999.0055","volume":"13","author":"A Metha","year":"2000","unstructured":"Metha A, Mason PJ, Vulliamy TJ (2000) Glucose-6-phosphate dehydrogenase deficiency. Baillieres Best Pract Res Clin Haematol 13:21\u201338","journal-title":"Baillieres Best Pract Res Clin Haematol"},{"key":"2124_CR5","doi-asserted-by":"crossref","first-page":"267","DOI":"10.1016\/j.blre.2007.05.002","volume":"21","author":"PJ Mason","year":"2007","unstructured":"Mason PJ, Bautista JM, Gilsanz F (2007) G6PD deficiency: the genotype-phenotype association. Blood Rev 21:267\u2013283","journal-title":"Blood Rev"},{"key":"2124_CR6","doi-asserted-by":"crossref","first-page":"871","DOI":"10.1136\/pgmj.70.830.871","volume":"70","author":"AB Mehta","year":"1994","unstructured":"Mehta AB (1994) Glucose 6-phosphate dehydrogenase deficiency. Postgrad Med 70:871\u2013877","journal-title":"Postgrad Med"},{"key":"2124_CR7","first-page":"1303","volume":"91","author":"L Luzzatto","year":"2006","unstructured":"Luzzatto L (2006) Glucose 6-phosphate dehydrogenase deficiency: from genotype to phenotype. Haematologica 91:1303\u20131306","journal-title":"Haematologica"},{"key":"2124_CR8","doi-asserted-by":"crossref","first-page":"3613","DOI":"10.1182\/blood.V84.11.3613.bloodjournal84113613","volume":"84","author":"E Beutler","year":"1994","unstructured":"Beutler E (1994) G6PD deficiency. Blood 84:3613\u20133636","journal-title":"Blood"},{"key":"2124_CR9","doi-asserted-by":"crossref","first-page":"260","DOI":"10.1016\/j.patbio.2007.08.009","volume":"56","author":"BB Daoud","year":"2008","unstructured":"Daoud BB, Mosbehi I, Pr\u00e9hu C et al (2008) Molecular characterization of erythrocyte glucose-6-phosphate deshydrogenase deficiency in Tunisia. Pathol Biol (Paris) 56:260\u2013267","journal-title":"Pathol Biol (Paris)"},{"key":"2124_CR10","doi-asserted-by":"crossref","first-page":"5171","DOI":"10.1073\/pnas.85.14.5171","volume":"85","author":"TJ Vulliamy","year":"1988","unstructured":"Vulliamy TJ, D\u2019ursot M, Battistuzzit G et al (1988) Diverse point mutations in the human glucose-6-phosphate dehydrogenase gene cause enzyme deficiency and mild or severe hemolytic anemia. Proc Natl Acad Sci USA 85:5171\u20135175","journal-title":"Proc Natl Acad Sci USA"},{"key":"2124_CR11","first-page":"391","volume":"42","author":"JL Vives Corrons","year":"1997","unstructured":"Vives Corrons JL, Zarza R, Aymerich JM et al (1997) Molecular analysis of glucose-6-dehydrogenase deficiency in Spain. Sangre (Barc) 42:391\u2013398","journal-title":"Sangre (Barc)"},{"key":"2124_CR12","first-page":"30","volume":"86","author":"A Pietrapertosa","year":"2001","unstructured":"Pietrapertosa A, Palma A, Campanale D et al (2001) Genotype and phenotype correlation in glucose-6-phosphate dehydrogenase deficiency. Haematologica 86:30\u201335","journal-title":"Haematologica"},{"key":"2124_CR13","doi-asserted-by":"crossref","first-page":"136","DOI":"10.1159\/000154342","volume":"46","author":"RA Bayoumi","year":"1996","unstructured":"Bayoumi RA, Nur-E-Kamal MS, Tadayyon M et al (1996) Molecular characterization of erythrocyte glucose-6-phosphate deshydrogenase deficiency in Al-Ain District, United Arab Emirates. Hum Hered 46:136\u2013141","journal-title":"Hum Hered"},{"key":"2124_CR14","doi-asserted-by":"crossref","first-page":"238","DOI":"10.1016\/S1079-9796(03)00038-X","volume":"30","author":"ST Saad","year":"2003","unstructured":"Saad ST, Costa FF (2003) Mild hemolysis in a girl with G6PD sumare (class I Variant) associated with G6PD A-. Blood Cells Mol Dis 30:238\u2013240","journal-title":"Blood Cells Mol Dis"},{"key":"2124_CR15","doi-asserted-by":"crossref","first-page":"141","DOI":"10.1016\/j.bcmd.2004.06.003","volume":"33","author":"S Sukumar","year":"2004","unstructured":"Sukumar S, Mukherjee MB, Colah RB et al (2004) Molecular basis of G6PD deficiency in India. Blood Cells Mol Dis 33:141\u2013145","journal-title":"Blood Cells Mol Dis"},{"key":"2124_CR16","doi-asserted-by":"crossref","first-page":"513","DOI":"10.1007\/BF00211017","volume":"94","author":"K Nafa","year":"1994","unstructured":"Nafa K, Reghis A, Osmani N et al (1994) At least five polymorphic mutants account for the prevalence of glucose-6-phosphate deshydrogenase in Algeria. Hum Genet 94:513\u2013517","journal-title":"Hum Genet"},{"issue":"1","key":"2124_CR17","first-page":"e2009005","volume":"1","author":"S Fattoum","year":"2009","unstructured":"Fattoum S (2009) Evolution of hemoglobinopathy prevention in Africa: results, problems and prospect. Medit J Hematol Infect Dis 1(1):e2009005","journal-title":"Medit J Hematol Infect Dis"},{"key":"2124_CR18","doi-asserted-by":"crossref","first-page":"127","DOI":"10.1016\/j.cccn.2003.10.022","volume":"340","author":"A Haj Khelil","year":"2004","unstructured":"Haj Khelil A, Laradi S, Miled A et al (2004) Clinical and molecular aspects of haemoglobinopathies in Tunisia. Clin Chim Acta 340:127\u2013137","journal-title":"Clin Chim Acta"},{"key":"2124_CR19","doi-asserted-by":"crossref","first-page":"66","DOI":"10.1111\/j.1365-2141.1995.tb05246.x","volume":"91","author":"A Rovira","year":"1995","unstructured":"Rovira A, Vulilamy T, Pujades M et al (1995) Molecular genetics of glucose-6-phosphate dehydrogenase (G6PD) deficiency in Spain: identification of two new point mutations in the G6PD gene. Br J Haematol 91:66\u201371","journal-title":"Br J Haematol"},{"key":"2124_CR20","doi-asserted-by":"crossref","first-page":"249","DOI":"10.1006\/bcmd.2002.0505","volume":"28","author":"MO Rodrigues","year":"2002","unstructured":"Rodrigues MO, Freire AP, Martins G et al (2002) Glucose-6-phosphate dehydrogenase deficiency in Portugal: biochemical and mutational profiles, heterogeneity, and haplotype association. Blood Cells Mol Dis 28:249\u2013259","journal-title":"Blood Cells Mol Dis"},{"key":"2124_CR21","first-page":"440","volume":"82","author":"F Martinez di Montemuros","year":"1997","unstructured":"Martinez di Montemuros F, Dotti C, Tavazzi D et al (1997) Molecular heterogeneity of glucose-6-phosphate dehydrogenase (G6PD) variants in Italy. Haematologica 82:440\u2013445","journal-title":"Haematologica"},{"key":"2124_CR22","doi-asserted-by":"crossref","first-page":"1605","DOI":"10.3923\/pjbs.2006.1605.1616","volume":"9","author":"M Magdy","year":"2006","unstructured":"Magdy M, El Humairy M, El Humairy AR (2006) Molecular characterization of new variants of glucose-6-phosphate deshydrogenase deficiency gene isolated in western province of Saudi Arabia causing hemolytic anemia. Pak J Biol Sci 9:1605\u20131616","journal-title":"Pak J Biol Sci"},{"key":"2124_CR23","doi-asserted-by":"crossref","first-page":"699","DOI":"10.1016\/j.clinbiochem.2007.02.008","volume":"40","author":"MR Noori-Daloii","year":"2007","unstructured":"Noori-Daloii MR, Hajebrahimi Z, Najafi L et al (2007) A comprehensive study on the major mutations in glucose-6-phosphate dehydrogenase-deficient polymorphic variants identified in the coastal provinces of Caspian Sea in the north of Iran. Clin Biochem 40:699\u2013704","journal-title":"Clin Biochem"},{"key":"2124_CR24","doi-asserted-by":"crossref","first-page":"455","DOI":"10.1126\/science.1061573","volume":"293","author":"SA Tishkoff","year":"2001","unstructured":"Tishkoff SA, Varkonyi R, Cahinhinan N et al (2001) Haplotype diversity and linkage disequilibrium at human G6PD: recent origin of alleles that confer malarial resistance. Science 293:455\u2013462","journal-title":"Science"},{"key":"2124_CR25","doi-asserted-by":"crossref","first-page":"16","DOI":"10.1182\/blood-2007-04-077412","volume":"111","author":"E Beutler","year":"2008","unstructured":"Beutler E (2008) Glucose-6-phosphate dehydrogenase deficiency: a historical perspective. Blood 111:16\u201324","journal-title":"Blood"},{"key":"2124_CR26","first-page":"81","volume":"37","author":"DK Chan","year":"2008","unstructured":"Chan DK (2008) Glucose-6-phosphate dehydrogenase deficiency: correlation between the genotype, biochemistry and phenotype. Ann Acad Med Singap 37:81\u201383","journal-title":"Ann Acad Med Singap"}],"container-title":["Molecular Biology Reports"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s11033-012-2124-8.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s11033-012-2124-8\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s11033-012-2124-8","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2020,7,14]],"date-time":"2020-07-14T21:50:27Z","timestamp":1594763427000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s11033-012-2124-8"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2012,10,14]]},"references-count":26,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2013,2]]}},"alternative-id":["2124"],"URL":"https:\/\/doi.org\/10.1007\/s11033-012-2124-8","relation":{},"ISSN":["0301-4851","1573-4978"],"issn-type":[{"value":"0301-4851","type":"print"},{"value":"1573-4978","type":"electronic"}],"subject":[],"published":{"date-parts":[[2012,10,14]]}}}