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Article

Is the G2019S LRRK2 mutation common in all southern European populations?

Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia - 1 Sept 2008

Papapetropoulos Spiridon, Adi Nikhil, Shehadeh Lina, Bishopric Nanette, Singer Carlos, Argyriou Andreas A, Chroni Elizabeth

Abstract excerpt

Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene, especially the G2019S mutation, have been identified as a common cause of Parkinson's disease in southern European and other Mediterranean populations (Iberians, Ashkenazi Jews and North African Arabs). Owing to the geographic and histor...

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Identifiers

PMID: 18617409
DOI: 10.1016/j.jocn.2007.08.013

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18617409-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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