Makino, M <br/><br/>
Mitochondrial DNA mutations in Leigh syndrome and their phylogenetic implications.  [electronic resource] 

 -  Journal of human genetics  2000 
 - 69-75 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1434-5161 
<br/><br/><label>Standard No.: </label>10.1007/s100380050014  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adenosine Triphosphatases--genetics<br/>Age of Onset<br/>Child<br/>Child, Preschool<br/>DNA Mutational Analysis<br/>DNA, Mitochondrial--genetics<br/>Electron Transport Complex IV--genetics<br/>Female<br/>Humans<br/>Infant<br/>Leigh Disease--enzymology<br/>Male<br/>Microscopy, Electron<br/>Muscle, Skeletal--pathology<br/>Phylogeny<br/>Point Mutation<br/>Polymerase Chain Reaction<br/>Polymorphism, Restriction Fragment Length<br/>Pyruvate Dehydrogenase Complex--genetics