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Article

The LRRK2 G2019S mutation in a series of Argentinean patients with Parkinson's disease: clinical and demographic characteristics.

Neuroscience letters - 14 Mar 2013

Gatto Emilia Mabel, Parisi Virginia, Converso Daniela Paola, Poderoso Juan José, Carreras María Cecilia, Martí-Massó José Felix, Paisán-Ruiz Coro

Abstract excerpt

OBJECTIVES: To determine clinical characteristics and frequency of leucine-rich repeat kinase 2 gene (LRRK2) mutations in a cohort of patients with Parkinson's disease (PD) from Argentina. BACKGROUND: Variation in the LRRK2 gene represents the most common genetic determinant of PD, only few data are available from Latin-America. DESIGN/METHODS: Informed consent was obtained and all studies were approved by the...

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PMID: 23340200
DOI: 10.1016/j.neulet.2013.01.011

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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