Molecular diagnosis of mitochondrial and nuclear DNA mutations among Egyption children with mitochondrial encephalomyopathies / Dina Ahmed Mehaney ; Supervised Fayza Abdelhamid Hassan , Sawsn Abdelhady Hassan , Randa Sabry
Material type: TextLanguage: eng Publication details: Cairo : Dina Ahmed Mehaney , 2009Description: 192P. : facsimiles ; 25cmOther title:- التشخيص الجزيئى للطفرات الجنينية فى الحمض النووى فى مرضى الأطفال المصريين المصابين بأمراض الميتوكوندريا العضلية والدماغية [Added title page title]
- Issued also as CD
Item type | Current library | Home library | Call number | Copy number | Status | Date due | Barcode | |
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Thesis | قاعة الرسائل الجامعية - الدور الاول | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.11.07.Ph.D.2009.Di.M (Browse shelf(Opens below)) | Not for loan | 01010110052745000 | |||
CD - Rom | مخـــزن الرســائل الجـــامعية - البدروم | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.11.07.Ph.D.2009.Di.M (Browse shelf(Opens below)) | 52745.CD | Not for loan | 01020110052745000 |
Thesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of Clinical and Chemical Pathology
Mitochondrial dysfuntion is one of the most common causes of pediatric Encephalomyopathies . Mitochondrial (mt) and Nuclear (n) Deoxyribonucleic acid (DNA) mutations are important causes of Encephalomyopathies . This study aimed at assessment of the frequency of these muations among 15 Egyption children clinically diagnosed as mitochondrial Encephalomyopathies
Issued also as CD
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