Gaig, Carles <br/><br/>
LRRK2 mutations in Spanish patients with Parkinson disease: frequency, clinical features, and incomplete penetrance.  [electronic resource] 

 -  Archives of neurology  Mar 2006 
 - 377-82 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0003-9942 
<br/><br/><label>Standard No.: </label>10.1001/archneur.63.3.377  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Age of Onset<br/>Aged<br/>Aged, 80 and over<br/>Arginine--genetics<br/>Child<br/>Child, Preschool<br/>DNA Mutational Analysis<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/>Pedigree<br/>Protein Serine-Threonine Kinases--genetics<br/>Serine--genetics<br/>Spain--epidemiology