Sirdah, Mahmoud; Sievertsen, Jürgen; Al-Yazji, Mansour S.; Tarazi, Issa S.; Al Haddad, Rami M.; Horstmann, Rolf D.; Timmann, Christian
(Elsevier, 2013)
Abstract
BACKGROUND:
β-Thalassemia is a disorder caused by mutations at the hemoglobin β-gene (HBB) locus. Its most important manifestation, the major form, is characterized by severe hypochromic and hemolytic anemia and ...