Zanna, Claudia <br/><br/>
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 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1460-2156 
<br/><br/><label>Standard No.: </label>10.1093/brain/awm335  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adenosine Triphosphate--biosynthesis<br/>Apoptosis--drug effects<br/>Cells, Cultured<br/>DNA Mutational Analysis--methods<br/>DNA, Mitochondrial--analysis<br/>Electron Transport<br/>Fibroblasts--drug effects<br/>GTP Phosphohydrolases--genetics<br/>Gene Deletion<br/>Humans<br/>Mitochondria--metabolism<br/>Optic Atrophy, Autosomal Dominant--genetics<br/>Oxidants--pharmacology<br/>Oxidative Phosphorylation<br/>Skin--metabolism