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...
Автор: | |
---|---|
Формат: | Дисертація |
Мова: | English |
Опубліковано: |
2011
|
Предмети: | |
Онлайн доступ: | http://psasir.upm.edu.my/id/eprint/21439/1/FPSK%28m%29_2011_22R.pdf |