Rouzier, Cécile <br/><br/>
The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype.  [electronic resource] 

 -  Brain : a journal of neurology  Jan 2012 
 - 23-34 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/awr323  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Child<br/>DNA Damage<br/>DNA, Mitochondrial--genetics<br/>Female<br/>GTP Phosphohydrolases--genetics<br/>Humans<br/>Male<br/>Middle Aged<br/>Mitochondrial Myopathies--complications<br/>Mitochondrial Proteins--genetics<br/>Mutation, Missense<br/>Optic Atrophy--complications<br/>Pedigree