Serum Hepcidin in Patients with β-Thalassemia Major
Abstract
β-thalassemia encompasses a group of monogenic diseases that have in common defective synthesis of β-globin. The defects involved are extremely heterogeneous and give rise to a large phenotypic spectrum, with patients that are almost asymptomatic to cases
Other data
| Title | Serum Hepcidin in Patients with β-Thalassemia Major | Other Titles | هرمون الهيبسيدين في مرضى أنيميا البحر المتوسط | Keywords | Serum Hepcidin in Patients with β-Thalassemia Major | Issue Date | 2012 | Description | β-thalassemia encompasses a group of monogenic diseases that have in common defective synthesis of β-globin. The defects involved are extremely heterogeneous and give rise to a large phenotypic spectrum, with patients that are almost asymptomatic to cases |
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