Yu-Wai-Man, Patrick <br/><br/>
OPA1 mutations impair mitochondrial function in both pure and complicated dominant optic atrophy.  [electronic resource] 

 -  Brain : a journal of neurology  Apr 2011 
 - e164 p.  digital 
<br/><br/> Publication Type: Letter; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1460-2156 
<br/><br/><label>Standard No.: </label>10.1093/brain/awq288  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Female<br/>GTP Phosphohydrolases--genetics<br/>Humans<br/>Male<br/>Middle Aged<br/>Mitochondria--genetics<br/>Mutation<br/>Optic Atrophy, Autosomal Dominant--genetics