Lesage, Suzanne <br/><br/>
Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans.  [electronic resource] 

 -  Human molecular genetics  May 2010 
 - 1998-2004 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1460-2083 
<br/><br/><label>Standard No.: </label>10.1093/hmg/ddq081  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Substitution--genetics<br/>Ethnicity--genetics<br/>Evolution, Molecular<br/>Haplotypes--genetics<br/>Humans<br/>Leucine-Rich Repeat Serine-Threonine Protein Kinase-2<br/>Mutation--genetics<br/>Parkinson Disease--genetics<br/>Protein Serine-Threonine Kinases--genetics