Serum Angiogenin level in Patients with Beta Thalassemia and Sickle Cell Disease
Ehab Kadees Sanad Bebawy;
Abstract
The β-Thalassemia syndromes are most common hereditary chronic hemolytic anemia due to impaired globin chain synthesis. This impairment leads to deficient hemoglobin resulting in hemolytic anemia.
Sickle cell disease is a genetic disorder which causes red
Sickle cell disease is a genetic disorder which causes red
Other data
| Title | Serum Angiogenin level in Patients with Beta Thalassemia and Sickle Cell Disease | Other Titles | مستوى الانجيوجينين في مصل مرضى أنيميا البحر المتوسط ومرضى أنيميا الخلايا المنجلية | Authors | Ehab Kadees Sanad Bebawy | Keywords | Serum Angiogenin level in Patients with Beta Thalassemia and Sickle Cell Disease | Issue Date | 2011 | Description | The β-Thalassemia syndromes are most common hereditary chronic hemolytic anemia due to impaired globin chain synthesis. This impairment leads to deficient hemoglobin resulting in hemolytic anemia. Sickle cell disease is a genetic disorder which causes red |
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