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The prevalence and molecular basis of beta-thalassemia in Isparta province and region

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dc.creator TUNC, B
dc.creator GUMRUK, F
dc.creator Cetin, Hasan
dc.creator ISTANBULLU, B
dc.creator YAVRUCUOGLU, H
dc.creator KURT, U
dc.creator GENC, H
dc.date 2001-12-31T22:00:00Z
dc.date.accessioned 2020-10-06T09:39:50Z
dc.date.available 2020-10-06T09:39:50Z
dc.identifier 33b50aec-021f-4bca-a8b4-ea5daa5f17f4
dc.identifier https://avesis.sdu.edu.tr/publication/details/33b50aec-021f-4bca-a8b4-ea5daa5f17f4/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/57034
dc.description The prevalence and molecular basis of beta-thalassemia in the district of Isparta were determined in a total of 6,054 healthy high school students who were recruited from 21 randomly selected high schools in the Isparta province and region. In 182 subjects, naked eye single tube red cell osmotic fragility test (NESTROFT test) was positive HbA(2) was measured by high-performance liquid chromatography (HPLC) in these subjects and was found to be high in 149 subjects. The incidence of beta-thalassemia was 149 in 6,054 (25076). The beta-thalassemia frequency was lower in the city center than in neighboring towns, 1.7% vs. 2.2%, respectively The most prevalent mutation of beta-thalassemia in this region was IVS 1-110 (G-A), followed by Codon 39 (C-T) and IVSII-745 (C-G).
dc.language eng
dc.rights info:eu-repo/semantics/closedAccess
dc.title The prevalence and molecular basis of beta-thalassemia in Isparta province and region
dc.type info:eu-repo/semantics/article


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