Coenzyme Q(10) defects may be associated with a deficiency of Q(10)-independent mitochondrial respiratory chain complexes

BACKGROUND: Coenzyme Q(10) (CoQ(10) or ubiquinone) deficiency can be due either to mutations in genes involved in CoQ(10) biosynthesis pathway, or to mutations in genes unrelated to CoQ(10) biosynthesis. CoQ(10) defect is the only oxidative phosphorylation disorder that can be clinically improved af...

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Detalles Bibliográficos
Publicado en:Biol Res
Main Authors: Fragaki, Konstantina, Chaussenot, Annabelle, Benoist, Jean-François, Ait-El-Mkadem, Samira, Bannwarth, Sylvie, Rouzier, Cécile, Cochaud, Charlotte, Paquis-Flucklinger, Véronique
Formato: Artigo
Idioma:Inglês
Publicado: BioMed Central 2016
Assuntos:
Research Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4705639/
https://ncbi.nlm.nih.gov/pubmed/26742794
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40659-015-0065-0
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