An Overview of Sickle Cell Disease and Its Treatments
Sickle cell disease (SCD) is a hereditary haemoglobinopathy resulting from a single point mutation in the β-globin gene (HBB) on chromosome 11, in which adenine is replaced by thymine at…
Sickle cell disease (SCD) is a hereditary haemoglobinopathy resulting from a single point mutation in the β-globin gene (HBB) on chromosome 11, in which adenine is replaced by thymine at…