Determination of alpha hemoglobin stabilizing protein (AHSP) gene expression and oxidative stress parameters in HbE/beta-Thalassemia
Beta-Thalassaemia is the genetic disorders of haemoglobin synthesis characterized by reduced or absent β-globin chain synthesis thus lead to imbalance of tetramer. The Alpha Haemoglobin Stabilizing Protein (AHSP) acts as a molecular chaperone for α-globin by stabilizing free α-globin preventing it f...
| المؤلف الرئيسي: | |
|---|---|
| التنسيق: | أطروحة |
| اللغة: | الإنجليزية |
| منشور في: |
2021
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| الموضوعات: | |
| الوصول للمادة أونلاين: | http://eprints.usm.my/50464/ |