Putative role of Bach1 gene in HbE/beta-thalassaemia patients
Beta thalassaemia is an autosomal blood disorder due to a quantitative reduction or total absence of beta globin chain synthesis caused by beta globin gene mutations. Haemoglobin E/ beta thalassaemia individuals have a diverse clinical severity due to globin chain imbalance and the effects of other...
Saved in:
主要作者: | Lee, Tze Yan |
---|---|
格式: | Thesis |
语言: | English |
出版: |
2013
|
主题: | |
在线阅读: | http://psasir.upm.edu.my/id/eprint/75309/1/FPSK%28M%29%202013%2047%20IR.pdf |
标签: |
添加标签
没有标签, 成为第一个标记此记录!
|
相似书籍
-
Molecular characterisation of beta thalassaemia in patients from Sabah, Malaysia
由: Teh, Lai Kuan
出版: (2014) -
Molecular genetics of HB E Beta-Thalassaemia /
由: Wong, Yean Ching
出版: (2005) -
Health-related quality of life and associated factors among patients with beta thalassemia attending three government hospitals in Selangor, Malaysia
由: Md Yusof, Asauji Yusnuryati
出版: (2011) -
Association of Alpha Haemoglobin Stabilizing Protein in HbE/ Beta-Thalassaemia Patients in Malaysia
由: Lim, Wai Feng
出版: (2011) -
Development of the amplification refractory mutation system (ARMS) for the analysis of rare beta thalassaemia mutations in Malaysia /
由: Chan, Yoke Fun
出版: (1999)