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 ten years, of all the potenti...
| Asıl Yazarlar: | , |
|---|---|
| Materyal Türü: | Makale |
| Dil: | English |
| Baskı/Yayın Bilgisi: |
Frontiers Media S.A.
2015-04-01
|
| Seri Bilgileri: | Frontiers in Genetics |
| Konular: | |
| Online Erişim: | http://journal.frontiersin.org/Journal/10.3389/fgene.2015.00134/full |