Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/22416
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dc.contributor.authorGeorgiou, I.en
dc.contributor.authorMakis, A.en
dc.contributor.authorChaidos, A.en
dc.contributor.authorBouba, I.en
dc.contributor.authorHatzi, E.en
dc.contributor.authorKranas, V.en
dc.contributor.authorZilidis, C.en
dc.contributor.authorBourantas, K. L.en
dc.date.accessioned2015-11-24T19:24:05Z-
dc.date.available2015-11-24T19:24:05Z-
dc.identifier.issn0902-4441-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/22416-
dc.rightsDefault Licence-
dc.subjectDNA Mutational Analysisen
dc.subjectGene Frequencyen
dc.subjectGenetic Testingen
dc.subjectGlobins/geneticsen
dc.subjectGreece/epidemiologyen
dc.subjectHumansen
dc.subject*Mutationen
dc.subjectTopography, Medicalen
dc.subjectbeta-Thalassemia/epidemiology/*geneticsen
dc.titleDistribution and frequency of beta-thalassemia mutations in northwestern and central Greeceen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/12581187-
heal.identifier.secondaryhttp://onlinelibrary.wiley.com/store/10.1034/j.1600-0609.2003.00017.x/asset/j.1600-0609.2003.00017.x.pdf?v=1&t=h2bonuxm&s=e22b196cfe18a6f6964beff9233d56a9f1aede9b-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.publicationDate2003-
heal.abstractOBJECTIVES: Beta-Thalassemia is a common autosomal recessive disorder resulting from over 200 different mutations of the beta-globin genes. The spectrum of beta-thalassemia mutations in Greece has been previously described in the population of the capital city of Athens, or in beta-thalassemia patients having transfusion therapy. The aim of the present study was to identify the distribution of the most common beta-thalassemia mutations in the population of northwestern and central Greece. METHODS: The data for this study were derived from a total of 1,130 unrelated subjects including 46 beta-thalassemia major, three beta -thalassemia intermedia and 1,081 carriers identified in our antenatal screening program. beta-Thalassemia mutations were identified by ARMS, DGGE and Reverse Dot Blot. RESULTS: The most common mutation, IVS-I-110, is followed, in order of frequency, by the mutations Cd-39, IVS-I-1, IVS-II-1, Cd-6, IVS-I-6, IVS-I-5, IVS-II-745, Cd-5 and 44 bp del. IVS-I-110 and Cd-39 frequencies are similar with those found in other Balkan countries. Significant differences in regional distribution were observed. The results showed a clear drift of the distribution of the most frequent IVS-I-110 mutation in the south-north (29.4, 40.0, 44.6 and 61.7%) and the east-west axis (31.8 and 44.6%). CONCLUSIONS: Population screening and prenatal diagnosis are significantly facilitated by these data. Furthermore, the detailed distribution tables of beta-thalassemia mutations are essential for counseling and extraction of genetic diversity estimates for population genetic studies in other inherited disorders.en
heal.journalNameEur J Haematolen
heal.journalTypepeer-reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ

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