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[Clinical features of LRRK2-associated Parkinson's disease].

Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova - 1 Jan 2011

Pchelina S N, Ivanova O N, Emel'ianov A K, Iakimovskiĭ A F

Abstract excerpt

Mutations in the Leucine Reach Repeat Kinase 2 (LRRK2) gene are the most frequent cause of familial Parkinson's disease (PD). Previously, we have sequenced the coding region of the LRRK2 gene in 85 PD patients and showed the prevalence of G2019S-associated PD (G2019S-PD) among all cases of LRRK2-associated PD in Russia. Screening of the most frequent LRRK2 mutations (G2019S, R1441C, R1441G) in the extended sample...

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PMID: 22433811

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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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