Zhao, Fuxin <br/><br/>
Leber's hereditary optic neuropathy is associated with mitochondrial ND6 T14502C mutation.  [electronic resource] 

 -  Biochemical and biophysical research communications  Nov 2009 
 - 466-72 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1090-2104 
<br/><br/><label>Standard No.: </label>10.1016/j.bbrc.2009.08.168  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Amino Acid Sequence<br/>Asian People--genetics<br/>Child, Preschool<br/>Female<br/>Humans<br/>Male<br/>Mitochondria--enzymology<br/>Molecular Sequence Data<br/>Mutation<br/>NADH Dehydrogenase--genetics<br/>Optic Atrophy, Hereditary, Leber--genetics<br/>Pedigree