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Nuclear gene mutations as the cause of mitochondrial complex III deficiency
Complex III (CIII) deficiency is one of the least common oxidative phosphorylation defects associated to mitochondrial disease. CIII constitutes the center of the mitochondrial respiratory chain, as well as a crossroad for several other metabolic pathways. For more than 10 years, of all the potentia...
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| Publicado no: | Front Genet |
|---|---|
| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Frontiers Media S.A.
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4391031/ https://ncbi.nlm.nih.gov/pubmed/25914718 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2015.00134 |
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