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Article

Association study of TREM2 polymorphism rs75932628 with leucoaraiosis or Parkinson's disease in the Han Chinese population.

BMJ open - 12 Jan 2016

Li Zhiming, Zhong Li, Gu Long, Huang Wenqing, Shi Xinzhen, Zhang Xilin, An Xingkai, Lin Qing, Tzeng Chi-Meng

Abstract excerpt

OBJECTIVES: The previously reported functional mutation rs75932628-T (p.R47H) in the triggering receptor expressed on myeloid cells 2 (TREM2) is a genetic risk factor for Alzheimer's disease, Parkinson's disease (PD) and frontotemporal dementia, in European populations. This study aims to assess the genetic association of the variant rs75932628-T with PD and leucoaraiosis (LA) in a Han Chinese population....

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Source

Open in PubMed Open full text

Identifiers

PMID: 26758262
DOI: 10.1136/bmjopen-2015-009499
PMCID: PMC4716257

Genes

TREM2

Provenance

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

Source receipt: pubmed, retrieved 5 Sept 2026.

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