Ameliorating β-thalassaemia by manipulating expression of the α-globin gene
<p>β-Thalassaemia is a disorder of haemoglobin production characterised by severe anaemia requiring life-long blood transfusions. The common genetic defects are predominantly based in and around the β-globin gene resulting in reduced or absent β-globin chain synthesis. The resultant excess of...
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| Μορφή: | Thesis |
| Γλώσσα: | English |
| Έκδοση: |
2015
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