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Article

An inherited small microdeletion at 15q13.3 in a patient with early-onset obsessive-compulsive disorder.

PloS one - 1 Jan 2014

Cappi Carolina, Hounie Ana Gabriela, Mariani Daniel B, Diniz Juliana Belo, Silva Aderbal R T, Reis Viviane N S, Busso Ariane F, Silva Amanda Gonçalves, Fidalgo Felipe, Rogatto Silvia Regina, Miguel Euripedes C, Krepischi Ana C, Brentani Helena

Abstract excerpt

Copy number variations (CNVs) have been previously associated with several different neurodevelopmental psychiatric disorders, such as autism, schizophrenia, and attention deficit hyperactivity disorder (ADHD). The present study consisted of a pilot genome-wide screen for CNVs in a cohort of 16 patients with early-onset obsessive-compulsive disorder (OCD) and 12 mentally healthy individuals, using array-based...

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Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 15

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to DNA Copy Number Variations

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Identifiers

PMID: 25303678
DOI: 10.1371/journal.pone.0110198
PMCID: PMC4193873

Genes

FMN1

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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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