The predominance of codon 39 (c>t) mutation of HBB gene in a portion of the Algerian population (Northeast Algeria)
This study was planned to determine the frequency of β-thalassemia mutations in Batna region (Northeast Algeria). Nineteen blood samples of clinically thalassemic children patients were collected from Department of Pediatrics, University Hospital of Batna. We carried out the molecular genetics of be...
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| Principais autores: | , , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
PAGEPress Publications
2017-04-01
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| Serija: | Journal of Biological Research |
| Teme: | |
| Online dostop: | http://www.pagepressjournals.org/index.php/jbr/article/view/6407 |
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