Gilles de la Tourette syndrome (GTS) is a complex neuropsychiatric disorder with a strong genetic influence where copy number variations are suggested to play a role in disease pathogenesis. In a previous small-scale copy number variation study of a GTS cohort (n = 111), recurrent exon-affecting microdeletions of four genes, including the gene encoding arylacetamide deacetylase (AADAC), were observed and merited further investigations.

Association of AADAC Deletion and Gilles de la Tourette Syndrome in a Large European Cohort

TOSATO, Sarah;
2016-01-01

Abstract

Gilles de la Tourette syndrome (GTS) is a complex neuropsychiatric disorder with a strong genetic influence where copy number variations are suggested to play a role in disease pathogenesis. In a previous small-scale copy number variation study of a GTS cohort (n = 111), recurrent exon-affecting microdeletions of four genes, including the gene encoding arylacetamide deacetylase (AADAC), were observed and merited further investigations.
2016
AADAC; Association study; CNV; Copy number variation; Gilles de la Tourette syndrome; Neuropsychiatric disorder; Adult; Animals; Attention Deficit Disorder with Hyperactivity; Cohort Studies; Comorbidity; DNA Copy Number Variations; Denmark; Exons; Female; Genotyping Techniques; Germany; Humans; Hungary; Iceland; Italy; Male; Mice; Netherlands; Sequence Deletion; Tourette Syndrome
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11562/950317
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