{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,5]],"date-time":"2026-03-05T06:57:32Z","timestamp":1772693852075,"version":"3.50.1"},"reference-count":20,"publisher":"Elsevier BV","issue":"2","license":[{"start":{"date-parts":[[2013,4,1]],"date-time":"2013-04-01T00:00:00Z","timestamp":1364774400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Pathologie Biologie"],"published-print":{"date-parts":[[2013,4]]},"DOI":"10.1016\/j.patbio.2012.03.005","type":"journal-article","created":{"date-parts":[[2012,4,30]],"date-time":"2012-04-30T22:41:40Z","timestamp":1335825700000},"page":"64-69","source":"Crossref","is-referenced-by-count":6,"title":["Three new mutations account for the prevalence of glucose 6 phosphate deshydrogenase (G6PD) deficiency in Tunisia"],"prefix":"10.1016","volume":"61","author":[{"given":"B.","family":"Bendaoud","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"I.","family":"Hosni","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"I.","family":"Mosbahi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"R.","family":"Hafsia","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C.","family":"Prehu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"S.","family":"Abbes","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.patbio.2012.03.005_bib0005","doi-asserted-by":"crossref","first-page":"177","DOI":"10.1007\/BF00272298","article-title":"Heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Algeria. Study in Northern Algeria with description of five new variants","volume":"40","author":"Benabadji","year":"1978","journal-title":"Hum Genet"},{"key":"10.1016\/j.patbio.2012.03.005_bib0010","doi-asserted-by":"crossref","first-page":"45","DOI":"10.1016\/S0268-960X(96)90019-3","article-title":"G6PD: population genetics and clinical manifestations","volume":"10","author":"Beutler","year":"1996","journal-title":"Blood Rev"},{"key":"10.1016\/j.patbio.2012.03.005_bib0015","doi-asserted-by":"crossref","first-page":"3953","DOI":"10.1182\/blood.V87.9.3953.bloodjournal8793953","article-title":"Multiple G6PD mutations are associated with a clinical and biochemical phenotype similar to that of G6PD Mediterranean","volume":"87","author":"Cappellini","year":"1996","journal-title":"Blood"},{"key":"10.1016\/j.patbio.2012.03.005_bib0020","doi-asserted-by":"crossref","first-page":"399","DOI":"10.1006\/bcmd.2002.0524","article-title":"Molecular heterogeneity of G6PD deficiency in an Amazonian population and description of four new variants","volume":"28","author":"Hamel","year":"2002","journal-title":"Blood Cells Mol Dis"},{"key":"10.1016\/j.patbio.2012.03.005_bib0025","doi-asserted-by":"crossref","first-page":"742","DOI":"10.1016\/j.clinbiochem.2007.11.009","article-title":"Glucose-6-phosphate dehydrogenase Buenos Aires: a novel de novo missense mutation associated with severe enzyme deficiency","volume":"41","author":"Minucci","year":"2008","journal-title":"Clin Biochem"},{"key":"10.1016\/j.patbio.2012.03.005_bib0030","doi-asserted-by":"crossref","first-page":"129","DOI":"10.1002\/jcla.20010","article-title":"Novel point mutation in exon 12 of the glucose-6-phosphate dehydrogenase gene: G6PD flores","volume":"18","author":"Rodrigues","year":"2004","journal-title":"J Clin Lab Anal"},{"key":"10.1016\/j.patbio.2012.03.005_bib0035","first-page":"49","article-title":"The first case of a class I glucose-6-phosphate dehydrogenase deficiency, G6PD Santiago de Cuba (1339 G>A), in a Chinese population as found in a survey for G6PD deficiency in northeastern and central China","volume":"64","author":"Wang","year":"2010","journal-title":"Acta Med Okayama"},{"key":"10.1016\/j.patbio.2012.03.005_bib0040","doi-asserted-by":"crossref","first-page":"988","DOI":"10.1016\/S0006-291X(05)81163-5","article-title":"Two commonly occurring nucleotide base substitutions in Chinese G6PD variants","volume":"180","author":"Chiu","year":"1991","journal-title":"Biochem Biophys Res Commun"},{"key":"10.1016\/j.patbio.2012.03.005_bib0045","doi-asserted-by":"crossref","first-page":"S154","DOI":"10.1002\/humu.1380110151","article-title":"G6PD Mount Sinai: a new severe hemolytic variant characterized by dual mutations at nucleotides 376G and 1159T (N126D)","volume":"Suppl1","author":"Vlachos","year":"1998","journal-title":"Hum Mutat"},{"key":"10.1016\/j.patbio.2012.03.005_bib0050","doi-asserted-by":"crossref","first-page":"257","DOI":"10.1182\/blood.V85.1.257.bloodjournal851257","article-title":"Glucose-6 phosphate dehydrogenase mutations and haplotypes in various ethnic groups","volume":"85","author":"Xu","year":"1995","journal-title":"Blood"},{"key":"10.1016\/j.patbio.2012.03.005_bib0055","doi-asserted-by":"crossref","first-page":"264","DOI":"10.1038\/sj.thj.6200042","article-title":"Molecular basis of haemoglobinopathies and G6PD deficiency in the Comorian population","volume":"1","author":"Badens","year":"2000","journal-title":"Hematol J"},{"key":"10.1016\/j.patbio.2012.03.005_bib0060","first-page":"9","article-title":"Glucose-6-phosphate dehydrogenase (G6PD) activity and deficiency in a population of Nigerian males resident in Jos, Niger","volume":"23","author":"Egesie","year":"2008","journal-title":"J Physiol Sci"},{"key":"10.1016\/j.patbio.2012.03.005_bib0065","doi-asserted-by":"crossref","first-page":"193","DOI":"10.1016\/j.clinbiochem.2009.09.012","article-title":"Rapid genotyping of two common G6PD variants, African (A-) and Mediterranean, by high-resolution melting analysis","volume":"43","author":"Joly","year":"2010","journal-title":"Clin Biochem"},{"key":"10.1016\/j.patbio.2012.03.005_bib0070","doi-asserted-by":"crossref","first-page":"8568","DOI":"10.1073\/pnas.88.19.8568","article-title":"Polymorphic sites in the African population detected by sequence analysis of the glucose-6-phosphate dehydrogenase gene outline the evolution of the variants A and A-","volume":"88","author":"Vulliamy","year":"1991","journal-title":"Proc Natl Acad Sci USA"},{"key":"10.1016\/j.patbio.2012.03.005_bib0075","doi-asserted-by":"crossref","first-page":"260","DOI":"10.1016\/j.patbio.2007.08.009","article-title":"Molecular characterization of erythrocyte glucose-6-phosphate dehydrogenase deficiency in Tunisia","volume":"56","author":"Daoud","year":"2008","journal-title":"Pathol Biol"},{"key":"10.1016\/j.patbio.2012.03.005_bib0080","doi-asserted-by":"crossref","first-page":"64","DOI":"10.1016\/S0140-6736(08)60073-2","article-title":"Glucose-6-phosphate dehydrogenase deficiency","volume":"371","author":"Cappellini","year":"2008","journal-title":"Lancet"},{"key":"10.1016\/j.patbio.2012.03.005_bib0085","doi-asserted-by":"crossref","first-page":"513","DOI":"10.1007\/BF00211017","article-title":"At least five polymorphic mutants account for the prevalence of glucose-6-phosphate dehydrogenase deficiency in Algeria","volume":"94","author":"Nafa","year":"1994","journal-title":"Hum Genet"},{"key":"10.1016\/j.patbio.2012.03.005_bib0090","doi-asserted-by":"crossref","first-page":"17","DOI":"10.1111\/j.1751-553X.2008.01108.x","article-title":"Frequency of Mediterranean mutation among a group of Saudi G6PD patients in Western region-Jeddah","volume":"32","author":"Gari","year":"2010","journal-title":"Int J Lab Hematol"},{"key":"10.1016\/j.patbio.2012.03.005_bib0095","doi-asserted-by":"crossref","first-page":"279","DOI":"10.1159\/000152815","article-title":"Distribution of G6PD types in the population of southwest France: common variants and new variants","volume":"26","author":"Gherardi","year":"1976","journal-title":"Hum Hered"},{"key":"10.1016\/j.patbio.2012.03.005_bib0100","doi-asserted-by":"crossref","first-page":"43","DOI":"10.1016\/S0009-8981(02)00098-0","article-title":"Identification of G6PD Mediterranean mutation by amplification refractory mutation system","volume":"321","author":"Maffi","year":"2002","journal-title":"Clin Chim Acta"}],"container-title":["Pathologie Biologie"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0369811412000417?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0369811412000417?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2020,7,6]],"date-time":"2020-07-06T23:17:32Z","timestamp":1594077452000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0369811412000417"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2013,4]]},"references-count":20,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2013,4]]}},"alternative-id":["S0369811412000417"],"URL":"https:\/\/doi.org\/10.1016\/j.patbio.2012.03.005","relation":{},"ISSN":["0369-8114"],"issn-type":[{"value":"0369-8114","type":"print"}],"subject":[],"published":{"date-parts":[[2013,4]]}}}