Molecular Analysis of β-Globin Mutations Among β-Thalassemia Patients in Hamadan
Background: β-Thalassemia (βT) is one of the most common genetic diseases. The specific mutation profile of that region can be identified by determining the specific mutations of each region and ethnicity. Objectives: This study investigated the β-globin mutations in patients with βT in Hamadan....
Kaydedildi:
| Asıl Yazarlar: | , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Hamadan University of Medical Sciences
2021-06-01
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| Seri Bilgileri: | Avicenna Journal of Medical Biochemistry |
| Konular: | |
| Online Erişim: | http://ajmb.umsha.ac.ir/PDF/ajmb-9-43.pdf |
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