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Article

Absence of association of the Ala58Val (rs17571) CTSD gene variant with Parkinson's disease or amyotrophic lateral sclerosis in a Han Chinese population.

Neuroscience letters - 1 Jan 2018

Xi Jing, Yang Xinglong, Zhao Quanzhen, Zheng Jinhua, An Ran, Tian Sijia, Huang Hongyan, Hu Fayunn, Ning Pingping, Xu Yanming

Abstract excerpt

Parkinson's disease (PD), amyotrophic lateral sclerosis (ALS) and Alzheimer's disease (AD) are neurodegenerative diseases that may share genetic risk factors. The exon variant Aal58Val (rs17571) in CTSD was recently associated with AD, leading us to examine whether it also affects risk of ALS and PD. The rs17571 variant was genotyped using the ligase detection reaction in 569 Han Chinese patients with PD, 301...

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Source

Identifiers

PMID: 28917980
DOI: 10.1016/j.neulet.2017.09.029

Genes

CTSD

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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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