β globin mutations in Turkish, Northern Iraqi and Albanian patients with β thalassemia major

The mutation detection of β thalassemia is absolutely necessary for molecular diagnosis, as well as any genetic epidemiological study. The β globin gene has 3 exons and 2 introns, involved in β-thalassemic pathogenesis. The study aim of the study is to characterize the spectrum of β globin gene muta...

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Autors principals:	Veysel Sabri Hancer, Tunc Fisgin, Murat Buyukdogan, Ceyhun Bozkurt, Sotiraq Lako
Format:	Artigo
Idioma:	Inglês
Publicat:	MDPI AG 2018-06-01
Col·lecció:	Thalassemia Reports
Matèries:	β globin mutations thalassemia major Turkey Northern Iraq Albania.
Accés en línia:	https://www.pagepressjournals.org/index.php/thal/article/view/7286
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