Description
Thalassemias and hemoglobinopathies are a group of hereditary diseases caused by quantitative or structural disorders in globin chains, the protein component of hemoglobin. Defects in hemoglobin synthesis lead to the development of anemia of varying severity with signs of hemolysis and iron overload in the body.
Period of execution
Within 13 days. The specified time does not include the day of biomaterial collection
Biomaterial type