Alpha-haemoglobin stabilising protein is a quantitative trait gene that modifies the phenotype of beta-thalassaemia.
It has been suggested that altered levels or function of alpha-haemoglobin stabilising protein (AHSP), an erythroid-specific protein that binds specifically to free alpha-(haemo)globin, might account for some of the clinical variability in beta-thalassaemia. To assess the variation of AHSP expressio...
Autori principali: | Lai, M, Jiang, J, Silver, N, Best, S, Menzel, S, Mijovic, A, Colella, S, Ragoussis, J, Garner, C, Weiss, M, Thein, S |
---|---|
Natura: | Journal article |
Lingua: | English |
Pubblicazione: |
2006
|
Documenti analoghi
Documenti analoghi
-
A novel quantitative trait locus controlling fetal haemoglobin on chromosome 2p15
di: Menzel, S, et al.
Pubblicazione: (2008) -
Haemoglobin E beta thalassaemia in Sri Lanka.
di: Premawardhena, A, et al.
Pubblicazione: (2005) -
Association of Alpha Haemoglobin Stabilizing Protein in HbE/ Beta-Thalassaemia Patients in Malaysia
di: Lim, Wai Feng
Pubblicazione: (2011) -
Haemoglobin Adana in alpha thalassaemia intermedia in the Malaysian population
di: Lee, Tze Yan
Pubblicazione: (2017) -
Genetic determinants of jaundice and gallstones in haemoglobin E beta thalassaemia.
di: Premawardhena, A, et al.
Pubblicazione: (2001)