Cock, H R <br/><br/>
Functional consequences of the 3460-bp mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.  [electronic resource] 

 -  Journal of the neurological sciences  May 1999 
 - 10-7 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/s0022-510x(99)00088-x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adenosine Triphosphate--biosynthesis<br/>Adult<br/>DNA, Mitochondrial--genetics<br/>Electron Transport--genetics<br/>Electron Transport Complex I<br/>Fibroblasts<br/>Humans<br/>Middle Aged<br/>Mitochondria, Muscle--chemistry<br/>Mutation--genetics<br/>NAD--metabolism<br/>NADH, NADPH Oxidoreductases--biosynthesis<br/>Optic Atrophies, Hereditary--genetics<br/>Reverse Transcriptase Polymerase Chain Reaction<br/>Rotenone--pharmacology<br/>Uncoupling Agents--pharmacology