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Glutathione S-transferase gene deletions and their effect on iron status in HbE/beta thalassemia patients
Annals of Hematology, 10/23/09
Sharma V et al. – Iron overload and oxidative stress are main pathophysiological features of HbE/eta thalassemia patients. Glutathione S–transferase genes (GSTT1 and GSTM1) are well known detoxification agents, and any mutation in the gene is known to cause oxidative damage. This is the first study to prove the role of GST gene deletions with iron overload in HbE/beta thalassemia.
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