Molecular spectrum of ?-globin gene mutations in the Aegean region of Turkey: first observation of three ?-globin gene mutations in the Turkish population
Küçük Resim Yok
Tarih
2015
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Springer Tokyo
Erişim Hakkı
info:eu-repo/semantics/closedAccess
Özet
Molecular test results of 231 individuals referred to our molecular genetics laboratory for analysis of ?-globin gene mutations between the years 2007 and 2013 were evaluated. Analysis of ?-thalassemia gene mutations was performed using reverse dot-blot hybridisation, which includes 21 common mutations. Twelve distinct ?-thalassemia mutations and 23 different genotypes have been detected in the Aegean region of Turkey. The most frequent mutations were –?3.7 (52.28 %), –(?)20.5 (14.74 %), --MED (10.53 %), and ?PA-1? (8.77 %). Three ?-thalassemia mutations (?cd142?, --SEA, and ?IC?), which are more prevalent in Southeast Asia, are identified for the first time in Turkey in this study. We find that a broad spectrum of ?-thalassemia mutations is present in the Aegean region of Turkey. The results obtained in this study may help inform decisions in the design and implementation of prevention strategies and diagnostic approaches. © 2015, The Japanese Society of Hematology.
Açıklama
Anahtar Kelimeler
Hemoglobinopathy, ?-globin gene, ?-thalassemia
Kaynak
International Journal of Hematology
WoS Q Değeri
Scopus Q Değeri
Q3
Cilt
102
Sayı
1
