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Article

P268S in NOD2 associates with susceptibility to Parkinson's disease in Chinese population.

Behavioral and brain functions : BBF - 7 May 2013

Ma Qilin, An Xingkai, Li Zhiming, Zhang Huanjing, Huang Wenqing, Cai Liangliang, Hu Peng, Lin Qing, Tzeng Chi-Meng

Abstract excerpt

BACKGROUND: The cause of almost all cases of Parkinson's disease (PD) remains unknown. Recent years have seen an explosion in the rate of discovery of genetic defects linked to PD. Different racial and geographical populations may have different distributions of genetic variants. METHODS: In the current study, we screened the following genetic variants, including some rare mutations and single nucleotide...

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Source

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Identifiers

PMID: 23651603
DOI: 10.1186/1744-9081-9-19
PMCID: PMC3662627

Genes

NOD2
SNCA

Variants

rs104893875
rs104893875
rs104893875
rs104893875
rs104893875

Provenance

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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