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...
CITATION STYLE
Al-Tubaikh, J. A. (2010). β-Thalassemia Major (Cooley’s Anemia). In Internal Medicine (pp. 293–296). Springer Berlin Heidelberg. https://doi.org/10.1007/978-3-642-03709-2_56
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