MOLECULAR DIAGNOSIS OF MITOCHONDRIAL AND NUCLEAR DNA MUTATIONS AMONG EGYPTION CHILDREN WITH MITOCHONDRIAL ENCEPHALOMYOPATHIES

Dina Ahmed Mehaney;

Abstract


Background :Mitochondrial dysfunction is one of the most common causes of pediatric Encephalomyopathies. Mitochondrial (mt) and Nuclear (n) Deoxyribonucleic acid (DNA) mutations are important causes of Encephalomyopathies.
Objectives. :This study ai

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Title MOLECULAR DIAGNOSIS OF MITOCHONDRIAL AND NUCLEAR DNA MUTATIONS AMONG EGYPTION CHILDREN WITH MITOCHONDRIAL ENCEPHALOMYOPATHIES
Other Titles التشخيص الجزيئي للطفرات الجينيه في الحمض النووي فى مرضي الأطفال المصريين المصابين بأمراض الميتوكوندريا العضليه والدماغيه
Authors Dina Ahmed Mehaney
Keywords MOLECULAR DIAGNOSIS OF MITOCHONDRIAL AND NUCLEAR DNA MUTATIONS AMONG EGYPTION CHILDREN WITH MITOCHONDRIAL ENCEPHALOMYOPATHIES
Issue Date 2009
Description 
Background :Mitochondrial dysfunction is one of the most common causes of pediatric Encephalomyopathies. Mitochondrial (mt) and Nuclear (n) Deoxyribonucleic acid (DNA) mutations are important causes of Encephalomyopathies.
Objectives. :This study ai

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