RBC alloimmunization in Egyptian blood transfusion- dependent β-thalassemia patients
Asmaa Mohammed Sayed Amer;
Abstract
The thalassemias are hereditary hemolytic anemias characterized by reduced or absent synthesis of one or more of the globin chains of hemoglobin leading to globin chain imbalance.
The most important forms of thalassemia result from autosomal mutant genes
The most important forms of thalassemia result from autosomal mutant genes
Other data
| Title | RBC alloimmunization in Egyptian blood transfusion- dependent β-thalassemia patients | Authors | Asmaa Mohammed Sayed Amer | Keywords | RBC alloimmunization in Egyptian blood transfusion- dependent β-thalassemia patients | Issue Date | 2007 | Description | The thalassemias are hereditary hemolytic anemias characterized by reduced or absent synthesis of one or more of the globin chains of hemoglobin leading to globin chain imbalance. The most important forms of thalassemia result from autosomal mutant genes |
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