Association of genetic variations in X-ray repair cross-complementing group 1 and Tourette syndrome.

doi:10.1002/jcla.21525

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Article

Association of genetic variations in X-ray repair cross-complementing group 1 and Tourette syndrome.

Journal of clinical laboratory analysis - 1 Sept 2012

Lin Wei-Yong, Lee Cheng-Chun, Liu Hsin-Ping, Chou I-Ching, Sheu Jim Jinn-Chyuan, Wan Lei, Lin Ying-Ju, Tsai Yuhsin, Tsai Fuu-Jen

Abstract excerpt

BACKGROUND: X-ray repair cross-complementing group 1 (XRCC1) plays a central role in mammalian DNA repair process. The polymorphism rs25487 (Arg>Gln at codon 399) of this gene is common in Han Chinese population. OBJECTIVES: The objective of this study was to analyze the association between this functional SNP of XRCC1 and Tourette syndrome (TS) in Han Taiwan Chinese population. METHODS: Genotyping was performed...

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PMID: 23001975
DOI: 10.1002/jcla.21525
PMCID: PMC6807472

Genes

XRCC1

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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