Doaa Mohammed Taher Abdelmohsen  <br/><br/>
Frequency of hemochromatosis (HFE ) gene mutations among B - thalassaemic patients with iron overload /  
 دراسة معدل الطفرات فى جين الهيموكروماتوزس فى مرضى الثلاثيما المعرضين لزيادة عنصر الحديد 
Doaa Mohammed Taher Abdelmohsen ; Supervised Magdy Ahmed Elsayed Ghoniem , Eman Moawad Mohammed Gouda , Nermeen Ahmed Eldesoukey 
 - Cairo :   Doaa Mohammed Taher Abdelmohsen ,   2010 
 - 126Leaves :   charts ;   30cm 
<br/><br/>Thesis (M.Sc.) - Cairo University - Faculty of Veterinary Medicine - Department of Biochemistry and Chemistry of Nutrition 
<br/><br/> Ý- thalassemia one of the most severe form of thalassemia is caused by defective globin production that causes anemia and also it results in iron overload which is the major cause of Ý- thalassemia mortality worldwide . Hereditary hemochromatosis is a disorder of iron metabolism characterized by increased iron intake and progressive storage and is related to mutations in the HFE gene 
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<br/><br/><label>Subjects--Index Terms: </label>Hemochromatosis (HFE ) gene  Hereditary hemochromatosis (HH )  Ý- thalassemia