OPA1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion.

Zanna, Claudia

OPA1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion. [electronic resource] - Brain : a journal of neurology Feb 2008 - 352-67 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

1460-2156

10.1093/brain/awm335 doi


Adenosine Triphosphate--biosynthesis
Apoptosis--drug effects
Cells, Cultured
DNA Mutational Analysis--methods
DNA, Mitochondrial--analysis
Electron Transport
Fibroblasts--drug effects
GTP Phosphohydrolases--genetics
Gene Deletion
Humans
Mitochondria--metabolism
Optic Atrophy, Autosomal Dominant--genetics
Oxidants--pharmacology
Oxidative Phosphorylation
Skin--metabolism