Association of Alpha Haemoglobin Stabilizing Protein in HbE/ Beta-Thalassaemia Patients in Malaysia
β-thalassaemia is a condition caused by the quantitative reduction or absence of β-globin chain synthesis due to β-globin gene mutations. It leads to excessive unpaired α-globin chains precipitates which causes membrane damage and ineffective erythropoiesis. Haemoglobin /β-thalassaemia patients have...
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| Format: | Thesis |
| Language: | English |
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2011
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| Online Access: | http://psasir.upm.edu.my/id/eprint/21439/1/FPSK%28m%29_2011_22R.pdf |