Molecular characterization of phenylketonuria mutation patterns in Egyptian patients / Mohamed Abdelhamid Elsayed Mohamed ; Supervised Adel Ali Kheir Eldin , Laila Kamal Effatt
Material type:
- التميز الجزيئى لأنماط طفرة الفينيل كيتونيوريا فى المرضى المصريين [Added title page title]
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قاعة الرسائل الجامعية - الدور الاول | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.08.01.M.Sc.2009.Mo.M (Browse shelf(Opens below)) | Not for loan | 01010110052389000 | ||
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مخـــزن الرســائل الجـــامعية - البدروم | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.08.01.M.Sc.2009.Mo.M (Browse shelf(Opens below)) | 52389.CD | Not for loan | 01020110052389000 |
Thesis (M.Sc.) - Cairo University - Faculty of Pharmacy - Department of Biochemistry
The present study was designed to analyze the phenylalanine hydroxylase (PAH) gene in 50 unrelated patients with phenylketonuria (PKU) to characterize the different mutations and polymorphisms that delineate the molecular genetic background of the disease in Egypt. It also aimed at providing a simple and cost - effective method for detecting the R176X mutation in exon 6. DNA was extracted from all patients using a standard procedure
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