Olsen, N K <br/><br/>
Leber's hereditary optic neuropathy associated with a disorder indistinguishable from multiple sclerosis in a male harbouring the mitochondrial DNA 11778 mutation.  [electronic resource] 

 -  Acta neurologica Scandinavica  May 1995 
 - 326-9 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0001-6314 
<br/><br/><label>Standard No.: </label>10.1111/j.1600-0404.1995.tb07016.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Base Composition--genetics<br/>Brain--pathology<br/>DNA Mutational Analysis<br/>DNA, Mitochondrial--genetics<br/>Electroencephalography<br/>Gene Frequency<br/>Humans<br/>Immunoglobulins--cerebrospinal fluid<br/>Magnetic Resonance Imaging<br/>Male<br/>Multiple Sclerosis--diagnosis<br/>Neurologic Examination<br/>Oligoclonal Bands<br/>Optic Atrophies, Hereditary--diagnosis<br/>Optic Nerve--pathology<br/>Pedigree