Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Fernández-Vizarra, Erika, Zeviani, Massimo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4391031/
https://www.ncbi.nlm.nih.gov/pubmed/25914718
http://dx.doi.org/10.3389/fgene.2015.00134

Ejemplares similares