ADVANCES IN THALASSEMIA MANAGEMENT AND CHELATION THERAPY
Autosomal recessive thalassemias are a heterogeneous group of diseases characterized by hypochromic microcytic anemia, which develops as a result of defective synthesis of one or more of the hemoglobin (Hb) chains. It occurs when the Hb chain or chains are produced in small numbers or not at all. In...
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| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2024-12-01
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| Series: | Hematology, Transfusion and Cell Therapy |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S2531137924029365 |
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