Mitochondrial coupling defect in Charcot-Marie-Tooth type 2A disease.

Loiseau, Dominique

Mitochondrial coupling defect in Charcot-Marie-Tooth type 2A disease. [electronic resource] - Annals of neurology Apr 2007 - 315-23 p. digital

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

0364-5134

10.1002/ana.21086 doi


Adenosine Triphosphate--metabolism
Adult
Apoptosis
Cells, Cultured
Charcot-Marie-Tooth Disease--complications
DNA Mutational Analysis
Female
Fibroblasts--metabolism
GTP Phosphohydrolases
Genetic Predisposition to Disease
Humans
Male
Membrane Potential, Mitochondrial--genetics
Membrane Proteins--genetics
Metabolic Networks and Pathways--physiology
Middle Aged
Mitochondrial Diseases--etiology
Mitochondrial Proteins--genetics
Mutation, Missense
Reactive Oxygen Species
Skin--pathology
Statistics, Nonparametric