Smith, P R <br/><br/>
Platelet mitochondrial function in Leber's hereditary optic neuropathy.  [electronic resource] 

 -  Journal of the neurological sciences  Mar 1994 
 - 80-3 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0022-510X 
<br/><br/><label>Standard No.: </label>10.1016/0022-510x(94)90055-8  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Blood Platelets--enzymology<br/>Citrate (si)-Synthase--blood<br/>DNA, Mitochondrial--metabolism<br/>Electron Transport Complex I<br/>Electron Transport Complex IV--blood<br/>Humans<br/>Mitochondria--enzymology<br/>Mutation<br/>NADH, NADPH Oxidoreductases--blood<br/>Optic Atrophies, Hereditary--blood<br/>Smoking--blood<br/>Succinate Cytochrome c Oxidoreductase--blood