Evaluation of Hepatic Enzymes in major β-thalassemic Patients using Deferasirox
Abstract β-thalassemia major is a genetic disease that causes sever defect in normal hemoglobin synthesis. The patients with β-thalassemia major need periodic blood transfusions that can result in accumulation of body iron, so treatment with iron chelating agent is required. Complications of this ir...
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| Format: | Book |
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College of Pharmacy University of Baghdad,
2022-12-01T00:00:00Z.
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A1234.567 |
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