Balicza, Péter <br/><br/>
[The absence of the common LRRK2 G2019S mutation in 120 young onset Hungarian Parkinon's disease patients].  [electronic resource] 

 -  Ideggyogyaszati szemle  Jul 2012 
 - 239-42 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0019-1442 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Age of Onset<br/>Aged<br/>Female<br/>Gene Frequency<br/>Genetic Predisposition to Disease<br/>Genetic Testing<br/>Glycine<br/>Humans<br/>Hungary--epidemiology<br/>Leucine-Rich Repeat Serine-Threonine Protein Kinase-2<br/>Male<br/>Middle Aged<br/>Parkinson Disease--epidemiology<br/>Point Mutation<br/>Protein Serine-Threonine Kinases--genetics<br/>Serine