A paradigm shift on beta-thalassaemia treatment: How will we manage this old disease with new therapies?
© 2018 The Authors Beta-thalassaemia causes defective haemoglobin synthesis leading to ineffective erythropoiesis, chronic haemolytic anaemia, and subsequent clinical complications. Blood transfusion and iron chelation allow long-term disease control, and haematopoietic stem cell transplantation off...
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| Main Authors: | , , , |
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| Other Authors: | |
| Format: | Review |
| Published: |
2019
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| Subjects: | |
| Online Access: | https://repository.li.mahidol.ac.th/handle/123456789/46572 |
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| Institution: | Mahidol University |
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