Kay, Denise M <br/><br/>
Validity and utility of a LRRK2 G2019S mutation test for the diagnosis of Parkinson's disease.  [electronic resource] 

 -  Genetic testing  2006 
 - 221-7 p.  digital 
<br/><br/> Publication Type: 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.; Validation Study 
<br/><br/><label>ISSN: </label>1090-6576 
<br/><br/><label>Standard No.: </label>10.1089/gte.2006.10.221  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Aged<br/>Aged, 80 and over<br/>Amino Acid Substitution--genetics<br/>Female<br/>Genetic Testing<br/>Humans<br/>Leucine-Rich Repeat Serine-Threonine Protein Kinase-2<br/>Male<br/>Middle Aged<br/>Parkinson Disease--diagnosis<br/>Protein Serine-Threonine Kinases--genetics<br/>Sensitivity and Specificity