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Article

LRRK2 gene variation and its contribution to Parkinson disease.

Human mutation - 1 Aug 2009

Paisán-Ruiz Coro

Abstract excerpt

Mutation in the LRRK2 gene is a known genetic cause of Parkinson disease (PD). However, due to the high frequency in which the most frequent LRRK2 mutation is present and the large size of LRRK2 gene, a complete sequence-based screening of the entire coding region has only been performed by a few researchers. In addition, normal variability in the LRRK2 gene has only been fully assessed in the North American...

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Identifiers

PMID: 19472409
DOI: 10.1002/humu.21038

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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