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https://hdl.handle.net/11499/4888
Title: | Beta-thalassemia mutations in Denizli province of Turkey | Authors: | Yildiz, S. Atalay, Ayfer Bağcı, Hüseyin Atalay, Erol Ömer |
Keywords: | Beta-thalassemia Mutation Turkey amino acid substitution article beta thalassemia codon ethnic difference gene mutation genetic disorder genetic heterogeneity hemolytic anemia human incidence major clinical study microcytosis Turkey (republic) |
Abstract: | Beta-thalassemia is one of the most common genetic disorders in Turkey as well as in several other Mediterranean countries presenting microcytosis and hemolytic anemia. The city of Denizli is located in the inner part of the Aegean geographical region of Turkey. The beta-thalassemia incidence in Denizli province is in between 2.6-3.7% reported by different researchers. According to our results; the IVS-1/nt-110 (G>A) is the most frequent mutation type in our province the same as other geographical regions of Turkey. Here we report also two HbD-Los Angeles/beta-thalassemia combinations, which are HbD-Los Angeles/codon 39 (C>T) and HbD-Los Angeles/IVS-1/nt-1 (G>A), respectively. In conclusion, our preliminary results show the heterogeneity of the beta-thalassemia mutations in the province of Denizli. | URI: | https://hdl.handle.net/11499/4888 | ISSN: | 1300-7777 |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu |
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