Abstract
β-thalassemia major is a hereditary hemolytic anemia, characterized by deficiency in the hemoglobin beta chain synthesis. Patients with β-thalassemia major are prone to repeated attacks of intravascular hemolysis that requires repeated hospitalization and blood transfusions.
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Al-Tubaikh, J.A. (2010). β-Thalassemia Major (Cooley's Anemia). In: Al-Tubaikh, J.A. (eds) Internal Medicine. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-03709-2_56
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DOI: https://doi.org/10.1007/978-3-642-03709-2_56
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-642-03708-5
Online ISBN: 978-3-642-03709-2
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