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Published in 2019 at "Heliyon"
DOI: 10.1016/j.heliyon.2019.e01905
Abstract: Sickle cell anaemia is a hereditary disease branded by an upsurge in generation of ROS, irregular iron release and little or no antioxidant activity which can lead to cellular injuries due to oxidative stress resulting…
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Keywords:
haemoglobin bisphosphoglycerate;
effects rutin;
bisphosphoglycerate mutase;
chemistry ... See more keywords