HbE and HbF levels in HbE/βO-thalassemia are heterogeneous
HbE/βO-thalassemia is the syndrome resulted from compound heterozygosity of HbE and βO-thalassemia alleles. The diagnosis of this condition relies on the detection of types and amounts of hemoglobin together with the evaluation of red blood cell morphology. The objective of the present study was to...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Chaing Mai University
2011-01-01
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| Series: | Journal of Associated Medical Sciences |
| Subjects: | |
| Online Access: | https://www.tci-thaijo.org/index.php/bulletinAMS/article/view/60043 |