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...

Повний опис

Бібліографічні деталі
Автор: Lim, Wai Feng
Формат: Дисертація
Мова:English
Опубліковано: 2011
Предмети:
Онлайн доступ:http://psasir.upm.edu.my/id/eprint/21439/1/FPSK%28m%29_2011_22R.pdf