Mitochondrial Disease: A Practical Approach for Primary Care Physicians
Abstract
Notorious variability in the presentation of mitochondrial disease in the infant and young child complicates its clinical diagnosis. Mitochondrial disease is not a single entity but, rather, a heterogeneous group of disorders characterized by impaired energy production due to genetically based oxidative phosphorylation dysfunction. Together, these disorders constitute the most common neurometabolic disease of childhood with an estimated minimal...
Paper Details
Title
Mitochondrial Disease: A Practical Approach for Primary Care Physicians
Published Date
Dec 1, 2007
Journal
Volume
120
Issue
6
Pages
1326 - 1333
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