Synofzik, Matthis <br/><br/>
POLG and PEO1 (Twinkle) mutations are infrequent in PSP-like atypical parkinsonism: a preliminary screening study.  [electronic resource] 

 -  Journal of neurology  Oct 2012 
 - 2232-3 p.  digital 
<br/><br/> Publication Type: Letter; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1432-1459 
<br/><br/><label>Standard No.: </label>10.1007/s00415-012-6535-1  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>DNA Helicases--genetics<br/>DNA Polymerase gamma<br/>DNA-Directed DNA Polymerase--genetics<br/>Female<br/>Genetic Testing<br/>Humans<br/>Male<br/>Middle Aged<br/>Mitochondrial Proteins--genetics<br/>Mutation<br/>Parkinsonian Disorders--genetics<br/>Phenotype