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
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- دراسة معدل الطفرات فى جين الهيموكروماتوزس فى مرضى الثلاثيما المعرضين لزيادة عنصر الحديد [Added title page title]
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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 | |||
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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 |
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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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