Please use this identifier to cite or link to this item: 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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