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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

By: Contributor(s): Material type: TextTextLanguage: 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]
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Dissertation note: Thesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of Clinical and Chemical Pathology Summary: 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
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Item type Current library Home library Call number Copy number Status Date due Barcode
Thesis 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 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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