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SLC6A3 rs28363170 and rs3836790 variants in Han Chinese patients with sporadic Parkinson's disease.

Neuroscience letters - 26 Aug 2016

Lu Qian, Song Zhi, Deng Xiong, Xiong Wei, Xu Hongbo, Zhang Zhenmei, Lu Hongwei, Deng Hao

Abstract excerpt

Parkinson's disease (PD; OMIM 168600) is the second most common neurodegenerative disorder characterized by the loss of dopamine-producing neurons in the substantia nigra and other brainstem nuclei. Recently, two variants (rs28363170 and rs3836790) in the solute carrier family 6 member 3 gene (SLC6A3) were identified to be significantly associated with PD patients in French population. The purpose of our study...

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PMID: 27353511
DOI: 10.1016/j.neulet.2016.06.053

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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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