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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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| Publicado en: | Biol Res |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
BioMed Central
2016
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| Assuntos: | |
| 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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