Ross, Owen A <br/><br/>
Corticobasal syndrome and primary progressive aphasia as manifestations of lrrk2 gene mutations.  [electronic resource] 

 -  Neurology  Jul 2008 
 - 303; author reply 303-4 p.  digital 
<br/><br/> Publication Type: Letter; Comment 
<br/><br/><label>ISSN: </label>1526-632X 
<br/><br/><label>Standard No.: </label>10.1212/01.wnl.0000320511.30222.dd  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aphasia, Primary Progressive--genetics<br/>Causality<br/>DNA Mutational Analysis--standards<br/>Genetic Markers--genetics<br/>Genetic Predisposition to Disease--genetics<br/>Genetic Testing--standards<br/>Genetic Variation--genetics<br/>Genotype<br/>Humans<br/>Inheritance Patterns--genetics<br/>Leucine-Rich Repeat Serine-Threonine Protein Kinase-2<br/>Mutation--genetics<br/>Neurodegenerative Diseases--genetics<br/>Norway<br/>Parkinson Disease--genetics<br/>Protein Serine-Threonine Kinases--genetics<br/>Risk Factors