Verny, C <br/><br/>
Multiple sclerosis-like disorder in OPA1-related autosomal dominant optic atrophy.  [electronic resource] 

 -  Neurology  Mar 2008 
 - 1152-3 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1526-632X 
<br/><br/><label>Standard No.: </label>10.1212/01.wnl.0000289194.89359.a1  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Brain--metabolism<br/>DNA Mutational Analysis<br/>Diagnosis, Differential<br/>Energy Metabolism--genetics<br/>GTP Phosphohydrolases--genetics<br/>Genetic Markers--genetics<br/>Genetic Predisposition to Disease--genetics<br/>Genotype<br/>Heterozygote<br/>Humans<br/>Magnetic Resonance Imaging<br/>Male<br/>Mitochondria--genetics<br/>Mitochondrial Diseases--genetics<br/>Multiple Sclerosis--genetics<br/>Mutation--genetics<br/>Nerve Fibers, Myelinated--metabolism<br/>Optic Atrophy, Autosomal Dominant--genetics<br/>Optic Nerve--metabolism