Identification of four common α-thalassemia gene deletions among a group with hemoglobinopathies in Sétif population, Algeria
α-Thalassemia (α-thal) is one of the most common genetic disorders in the world. It is characterized by the absence or reduced expression of α-globin genes. This study was carried out to evaluate the allelic frequency of α-thal defects in a patient for the first time in Sétif (Algeria). One hundred...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
De Gruyter
2013-12-01
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| Series: | Pteridines |
| Subjects: | |
| Online Access: | https://doi.org/10.1515/pterid-2013-0034 |