Biochemical Assessment of Coenzyme Q10 Deficiency
Abstract
Coenzyme Q10 (CoQ10) deficiency syndrome includes clinically heterogeneous mitochondrial diseases that show a variety of severe and debilitating symptoms. A multiprotein complex encoded by nuclear genes carries out CoQ10 biosynthesis. Mutations in any of these genes are responsible for the primary CoQ10 deficiency, but there are also different conditions that induce secondary CoQ10 deficiency including mitochondrial DNA (mtDNA) depletion and...
Paper Details
Title
Biochemical Assessment of Coenzyme Q10 Deficiency
Published Date
Mar 5, 2017
Journal
Volume
6
Issue
3
Pages
27 - 27
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