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Article

The G2019S LRRK2 mutation is rare in Korean patients with Parkinson's disease.

The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques - 1 Feb 2007

Cho Jin-Whan, Kim Sung-Yeon, Park Sung-Sup, Kim Han-Jun, Ahn Tae-Beom, Kim Jong-Min, Jeon Beom-Seok

Abstract excerpt

BACKGROUND: A number of causative mutations such as alpha-synuclein, parkin, UCHL1, Pink-1, DJ-1 have been identified in Parkinson's disease (PD). They are usually found in the familial cases. One mutation of great interest is the G2019S mutation in the LRRK2 gene, which has been reported in both familial and sporadic PD. Its prevalence has been reported to vary markedly among different races. We examined the...

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Source

Identifiers

PMID: 17352347
DOI: 10.1017/s0317167100005783

Genes

UCHL1

Provenance

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.

Related research

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The G2019S LRRK2 mutation is rare in Korean patients with Parkinson's disease.PMID 17352347Read ↗

The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients.Semantic proximity Read ↗

G2019S mutation of the leucine-rich repeat kinase 2 gene in a cohort of Egyptian patients with Parkinson's disease.Semantic proximity Read ↗

Mutations in LRRK2 other than G2019S are rare in a north American-based sample of familial Parkinson's disease.Semantic proximity Read ↗

Identification and haplotype analysis of LRRK2 G2019S in Japanese patients with Parkinson disease.Semantic proximity Read ↗

Frequency and phenotypes of LRRK2 G2019S mutation in Italian patients with Parkinson's disease.Semantic proximity Read ↗

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

LRRK2 mutations and risk variants in Japanese patients with Parkinson's disease.Semantic proximity Read ↗

A study of LRRK2 mutations and Parkinson's disease in Brazil.Semantic proximity Read ↗

The G2019S LRRK2 mutation is uncommon amongst Greek patients with sporadic Parkinson's disease.Semantic proximity Read ↗

Analysis of the LRRK2 p.G2019S mutation in Colombian Parkinson's Disease Patients.Semantic proximity Read ↗

A Korean Parkinson's disease family with the LRRK2 p.Tyr1699Cys mutation showing clinical heterogeneity.Semantic proximity Read ↗

LRRK2 G2019S mutation does not contribute to Parkinson's disease in South India.Semantic proximity Read ↗

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