Association of Alpha Haemoglobin Stabilizing Protein in HbE/ Beta-Thalassaemia Patients in Malaysia

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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書目詳細資料
主要作者:	Lim, Wai Feng
格式:	Thesis
語言:	English
出版:	2011
主題:	Thalassemia - blood Thalassemia - Diagnosis
在線閱讀:	http://psasir.upm.edu.my/id/eprint/21439/1/FPSK%28m%29_2011_22R.pdf
標簽:	添加標簽沒有標簽, 成為第一個標記此記錄!

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