New Insights in β-Thalassaemia
Thalassaemia is a hereditary cause of hypochromic microcytic anaemia resulting from defects in haemoglobin production. β-thalassaemia, which is caused by a decrease in the production of β-globin chains, affects multiple organs and is associated with considerable morbidity and mortality. This review...
| Main Authors: | , |
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| Format: | Article |
| Language: | English |
| Published: |
European Medical Journal
2019-08-01
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| Series: | European Medical Journal Hematology |
| Subjects: | |
| Online Access: | https://www.emjreviews.com/hematology/article/editors-pick-new-insights-in-%ce%b2-thalassaemia/ |