Riggs, J E <br/><br/>
Acute periaqueductal syndrome associated with the G11778A mitochondrial DNA mutation.  [electronic resource] 

 -  Neurology  Feb 2001 
 - 570-1 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0028-3878 
<br/><br/><label>Standard No.: </label>10.1212/wnl.56.4.570  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>DNA, Mitochondrial--genetics<br/>Humans<br/>Magnetic Resonance Imaging<br/>Male<br/>Mutation--genetics<br/>Neurodegenerative Diseases--genetics<br/>Optic Atrophies, Hereditary--genetics<br/>Periaqueductal Gray--pathology<br/>Syndrome