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Article

Worldwide frequency of G2019S LRRK2 mutation in Parkinson's disease: a systematic review.

Parkinsonism & related disorders - 1 May 2010

Correia Guedes L, Ferreira J J, Rosa M M, Coelho M, Bonifati V, Sampaio C

Abstract excerpt

BACKGROUND: The LRRK2 G2019S mutation is the most frequent known cause of familial and sporadic Parkinson's disease. Knowledge of its worldwide frequency distribution is essential for clinical and molecular research as well as genetic counseling. OBJECTIVES: To conduct a systematic review of the reported frequency of G2019S in different populations and to assess critically the quality of the clinical studies....

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Identifiers

PMID: 19945904
DOI: 10.1016/j.parkreldis.2009.11.004

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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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Worldwide frequency of G2019S LRRK2 mutation in Parkinson's disease: a systematic review.PMID 19945904Read ↗

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