Ishihara, Lianna <br/><br/>
Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutations.  [electronic resource] 

 -  Archives of neurology  Sep 2006 
 - 1250-4 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S. 
<br/><br/><label>ISSN: </label>0003-9942 
<br/><br/><label>Standard No.: </label>10.1001/archneur.63.9.1250  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>DNA Mutational Analysis--methods<br/>Family Health<br/>Female<br/>Gene Frequency<br/>Genetic Predisposition to Disease<br/>Glycine--genetics<br/>Humans<br/>Leucine-Rich Repeat Serine-Threonine Protein Kinase-2<br/>Male<br/>Middle Aged<br/>Mutation<br/>Parkinson Disease--epidemiology<br/>Protein Serine-Threonine Kinases--genetics<br/>Serine--genetics