Abnormal red blood cell morphological changes in thalassaemia associated with iron overload and oxidative stress
AimsIron overload is a major factor contributing to the overall pathology of thalassaemia, which is primarily mediated by ineffective erythropoiesis and shorter mature red blood cell (RBC) survival. Iron accumulation in RBCs generates reactive oxygen species (ROS) that cause cellular damage such as...
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Published in | Journal of clinical pathology Vol. 72; no. 8; pp. 520 - 524 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
BMJ Publishing Group LTD
01.08.2019
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Subjects | |
Online Access | Get full text |
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