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:
Main Author: | Lee, Tze Yan |
---|---|
Format: | Thesis |
Language: | English |
Published: |
2013
|
Subjects: | |
Online Access: | http://psasir.upm.edu.my/id/eprint/75309/1/FPSK%28M%29%202013%2047%20IR.pdf |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Molecular characterisation of beta thalassaemia in patients from Sabah, Malaysia
by: Teh, Lai Kuan
Published: (2014) -
Molecular genetics of HB E Beta-Thalassaemia /
by: Wong, Yean Ching
Published: (2005) -
Health-related quality of life and associated factors among patients with beta thalassemia attending three government hospitals in Selangor, Malaysia
by: Md Yusof, Asauji Yusnuryati
Published: (2011) -
Association of Alpha Haemoglobin Stabilizing Protein in HbE/ Beta-Thalassaemia Patients in Malaysia
by: Lim, Wai Feng
Published: (2011) -
Development of the amplification refractory mutation system (ARMS) for the analysis of rare beta thalassaemia mutations in Malaysia /
by: Chan, Yoke Fun
Published: (1999)