Molecular Investigation of Beta Globin Gene Cluster Deletions in Anemic Patients Referred to the Genetic Laboratory of Amirkola Children Hospital (Iran)
BACKGROUND AND OBJECTIVE: Hereditary persistence of fetal hemoglobin (HPFH) and δβ-thalassemia are heterogeneous disorders characterized by elevated levels of fetal hemoglobin (Hb F). Deletional mutations are responsible for the disease and are not recognized by routine hematological tests. The aim...
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| Auteurs principaux: | , , , , , , , |
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| Format: | article |
| Langue: | EN FA |
| Publié: |
Babol University of Medical Sciences
2012
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| Accès en ligne: | https://doaj.org/article/81fc2834a09f4abdb83e659b12c69211 |
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