Hashad, Doaa I <br/><br/>
G2019S mutation of the leucine-rich repeat kinase 2 gene in a cohort of Egyptian patients with Parkinson's disease.  [electronic resource] 

 -  Genetic testing and molecular biomarkers  Dec 2011 
 - 861-6 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1945-0257 
<br/><br/><label>Standard No.: </label>10.1089/gtmb.2011.0016  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>Cohort Studies<br/>DNA Mutational Analysis<br/>Egypt--epidemiology<br/>Female<br/>Gene Frequency<br/>Genetic Predisposition to Disease<br/>Humans<br/>Leucine-Rich Repeat Serine-Threonine Protein Kinase-2<br/>Male<br/>Middle Aged<br/>Mutation<br/>Parkinson Disease--diagnosis<br/>Polymerase Chain Reaction--methods<br/>Polymorphism, Restriction Fragment Length<br/>Prevalence<br/>Protein Serine-Threonine Kinases--genetics<br/>Severity of Illness Index