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Article

Intragenic deletions affecting two alternative transcripts of the IMMP2L gene in patients with Tourette syndrome.

European journal of human genetics : EJHG - 1 Nov 2014

Bertelsen Birgitte, Melchior Linea, Jensen Lars R, Groth Camilla, Glenthøj Birte, Rizzo Renata, Debes Nanette Mol, Skov Liselotte, Brøndum-Nielsen Karen, Paschou Peristera, Silahtaroglu Asli, Tümer Zeynep

Abstract excerpt

Tourette syndrome is a neurodevelopmental disorder characterized by multiple motor and vocal tics, and the disorder is often accompanied by comorbidities such as attention-deficit hyperactivity-disorder and obsessive compulsive disorder. Tourette syndrome has a complex etiology, but the underlying environmental and genetic factors are largely unknown. IMMP2L (inner mitochondrial membrane peptidase, subunit 2)...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 24549057
DOI: 10.1038/ejhg.2014.24
PMCID: PMC4200436

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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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