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...
Saved in:
| Main Authors: | , , , , , , , |
|---|---|
| Format: | article |
| Language: | EN FA |
| Published: |
Babol University of Medical Sciences
2012
|
| Subjects: | |
| Online Access: | https://doaj.org/article/81fc2834a09f4abdb83e659b12c69211 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|