Historique
M. KARIMI ;
LAHSAEIZADEH S. ;
JAFARI H. ;
SALAMI Z.
|
2008
Dans Journal of Substance Use (Vol.13 n°5, 2008) Article : Périodique
Dans Journal of Substance Use (Vol.13 n°5, 2008) Article : Périodique
ENGLISH :
Objective: Beta thalassemia is a hereditary disease of hemoglobin synthesis that causes mild to severe microcytic anemia and hemosiderosis in many organs that in severe cases results in organ failure. Many of the patients need blood [...]
