Molecular Characterisation of Alpha-Thalassaemia in Patients Investigated for Hypochromic Microcytic Indices in Hospital Universiti Sains Malaysia
Alpha (α)-thalassaemia is a common genetic disorder that affects 5 % of the worldwide population. Deletional or non-deletional mutations of one or both HBA1 and HBA2 on chromosome 16 cause a reduction/abnormal in the production of α globin chains, a component of haemoglobin (Hb) which are require...
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| 格式: | Thesis |
| 语言: | English |
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2023
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| 在线阅读: | http://eprints.usm.my/58801/1/03-DIVASHINI%20AP%20VIJIAN-FINAL%20THESIS%20P-SGM000820%28R%29-24%20pages.pdf |
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