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Article

Tourette syndrome is associated with recurrent exonic copy number variants.

Neurology - 18 May 2010

Sundaram Senthil K, Huq Ahm M, Wilson Benjamin J, Chugani Harry T

Abstract excerpt

BACKGROUND: Multiple rare copy number variants (CNVs) including genomic deletions and duplications play a prominent role in neurodevelopmental disorders such as mental retardation, autism, and schizophrenia, but have not been systematically studied in Tourette syndrome (TS). METHODS: We performed a genome-wide screening of single nucleotide polymorphism (SNP) genotyping microarray data to identify recurrent or de...

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Identifiers

PMID: 20427753
DOI: 10.1212/WNL.0b013e3181e0f147
PMCID: PMC2876824

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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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