Taylor, Robert W <br/><br/>
Leigh disease associated with a novel mitochondrial DNA ND5 mutation.  [electronic resource] 

 -  European journal of human genetics : EJHG  Feb 2002 
 - 141-4 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1018-4813 
<br/><br/><label>Standard No.: </label>10.1038/sj.ejhg.5200773  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Child<br/>DNA, Mitochondrial--genetics<br/>Humans<br/>Leigh Disease--etiology<br/>Male<br/>Mutation, Missense<br/>Sequence Analysis, DNA