Defects in the gene encoding β-globin, a component of adult haemoglobin, cause β-globinopathies such as sickle cell disease and β-thalassaemia. Disease symptoms can be alleviated by the induction of ...
THE typical case of spontaneously occurring pyridoxine-responsive anemia in human beings has been characterized by hypochromic, microcytic red cells, normoblastic proliferation in the bone marrow, ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results