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Frequency of hemochromatosis (HFE ) gene mutations among B - thalassaemic patients with iron overload / Doaa Mohammed Taher Abdelmohsen ; Supervised Magdy Ahmed Elsayed Ghoniem , Eman Moawad Mohammed Gouda , Nermeen Ahmed Eldesoukey

By: Contributor(s): Material type: TextTextLanguage: eng Publication details: Cairo : Doaa Mohammed Taher Abdelmohsen , 2010Description: 126Leaves : charts ; 30cmOther title:
  • دراسة معدل الطفرات فى جين الهيموكروماتوزس فى مرضى الثلاثيما المعرضين لزيادة عنصر الحديد [Added title page title]
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Dissertation note: Thesis (M.Sc.) - Cairo University - Faculty of Veterinary Medicine - Department of Biochemistry and Chemistry of Nutrition Summary: 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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Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.10.04.M.Sc.2010.Do.F (Browse shelf(Opens below)) Not for loan 01010110053320000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.10.04.M.Sc.2010.Do.F (Browse shelf(Opens below)) 53320.CD Not for loan 01020110053320000

Thesis (M.Sc.) - Cairo University - Faculty of Veterinary Medicine - Department of Biochemistry and Chemistry of Nutrition

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

Issued also as CD

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