Pfeffer, Gerald <br/><br/>
Clinical features of MS associated with Leber hereditary optic neuropathy mtDNA mutations.  [electronic resource] 

 -  Neurology  Dec 2013 
 - 2073-81 p.  digital 
<br/><br/> Publication Type: Journal Article; Meta-Analysis; Research Support, Non-U.S. Gov't; Review 
<br/><br/><label>ISSN: </label>1526-632X 
<br/><br/><label>Standard No.: </label>10.1212/01.wnl.0000437308.22603.43  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Cohort Studies<br/>DNA, Mitochondrial--genetics<br/>Female<br/>Humans<br/>Male<br/>Multiple Sclerosis--diagnosis<br/>Mutation--genetics<br/>Optic Atrophy, Hereditary, Leber--diagnosis<br/>Prospective Studies<br/>United Kingdom--epidemiology<br/>Young Adult