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LRRK2 mutations in patients with Parkinson's disease from Peru and Uruguay

✍ Scribed by Ignacio F. Mata; Carlos Cosentino; Victoria Marca; Luis Torres; Pilar Mazzetti; Olimpio Ortega; Victor Raggio; Ruth Aljanati; Ricardo Buzó; Dora Yearout; Elena Dieguez; Cyrus P. Zabetian

Book ID
116820581
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
183 KB
Volume
15
Category
Article
ISSN
1353-8020

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## Abstract Mutations in the leucine‐rich repeat kinase 2 (__LRRK2__) gene are the most common genetic determinant of Parkinson's disease (PD) in European‐derived populations, but far less is known about __LRRK2__ mutations and susceptibility alleles in Asians. To address this issue, we sequenced t