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Article

Genetic analysis of P387L mutation in SLC18A2 gene in sporadic Parkinson's disease in Chinese Han population.

Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences - 1 Aug 2015

Kang Jifeng, Tang Beisha, Li Kai, Liu Zhenhua, Yan Xinxiang, Guo Jifeng

Abstract excerpt

OBJECTIVE: To investigate whether the mutation of P387L in SLC18A2 gene is a cause for sporadic Parkinson's disease (PD) in Chinese Han population. METHODS: A total of 931 subjects (455 sporadic PD patients and 476 healthy controls) were enrolled in our study. SLC18A2 P387L was genotyped by matrix-assisted laser desorption/ionization-time-of-flight mass spectrometry (MALDI-TOF MS) and the results were verified by...

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PMID: 26333488
DOI: 10.11817/j.issn.1672-7347.2015.08.001

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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