Analysis of beta globin gene mutations in Diyarbakir

Hemoglobin disorders are quite heterogeneous in the Turkish population. Up to now, more than forty different beta thalassemia mutations and 60 hemoglobin variants have been characterized in the country. The aim of this study was to investigate genetic heterogeneity of HBB gene mutations in patients...

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Veröffentlicht in:	Türk biyokimya dergisi 2021-11, Vol.47 (1), p.113-118
Hauptverfasser:	Tekeş, Selahaddin, Oral, Diclehan, Söker, Murat, Şimşek, Selda, Uzel, Veysiye Hülya, Çürük, Mehmet Akif
Format:	Artikel
Sprache:	eng
Schlagworte:	Güneydoğu Anadolu Bölgesi HBB:c.208G>A HBB:c.34G>A southeastern Anatolia region talasemi β-talasemi β-thalassemia
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Beschreibung
Zusammenfassung:	Hemoglobin disorders are quite heterogeneous in the Turkish population. Up to now, more than forty different beta thalassemia mutations and 60 hemoglobin variants have been characterized in the country. The aim of this study was to investigate genetic heterogeneity of HBB gene mutations in patients and their parents at Southeastern Anatolia in Turkey.
ISSN:	1303-829X 1303-829X
DOI:	10.1515/tjb-2020-0546