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
Autores principales: Fragaki, Konstantina, Chaussenot, Annabelle, Benoist, Jean-François, Ait-El-Mkadem, Samira, Bannwarth, Sylvie, Rouzier, Cécile, Cochaud, Charlotte, Paquis-Flucklinger, Véronique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4705639/
https://www.ncbi.nlm.nih.gov/pubmed/26742794
http://dx.doi.org/10.1186/s40659-015-0065-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4705639/
https://www.ncbi.nlm.nih.gov/pubmed/26742794
http://dx.doi.org/10.1186/s40659-015-0065-0

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