Invertebrate Models for Coenzyme Q(10) Deficiency

The human syndrome of coenzyme Q (CoQ) deficiency is a heterogeneous mitochondrial disease characterized by a diminution of CoQ content in cells and tissues that affects all the electron transport processes CoQ is responsible for, like the electron transference in mitochondria for respiration and AT...

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Bibliographic Details
Main Authors: Fernández-Ayala, Daniel J.M., Jiménez-Gancedo, Sandra, Guerra, Ignacio, Navas, Plácido
Format: Artigo
Language:Inglês
Published: S. Karger AG 2014
Subjects:
Published online: May, 2014
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC4112529/
https://ncbi.nlm.nih.gov/pubmed/25126050
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000362751
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