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Article

An association analysis of the R1628P and G2385R polymorphisms of the LRRK2 gene in multiple system atrophy in a Chinese population.

Parkinsonism & related disorders - 1 Feb 2015

Yuan XiaoQin, Chen YongPing, Cao Bei, Zhao Bi, Wei QianQian, Guo XiaoYan, Yang Yuan, Yuan LiXing, Shang HuiFang

Abstract excerpt

BACKGROUND: Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene have been reported to be responsible for autosomal dominant late-onset sporadic Parkinson's disease (PD). The R1628P and G2385R polymorphisms of the LRRK2 gene have been identified as exclusively associated with PD in Asian po...

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PMID: 25511328
DOI: 10.1016/j.parkreldis.2014.11.022

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MAF

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Prepared record publication-25511328-2026-09-05.1. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 5 Sept 2026.

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