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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Detalhes bibliográficos
Publicado no: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 em: BioMed Central 2016
Assuntos:
Research Article
Acesso em linha: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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