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Article

Executive functions and memory abilities in children with 22q11.2 deletion syndrome.

The Australian and New Zealand journal of psychiatry - 1 Apr 2010

Campbell Linda E, Azuma Rayna, Ambery Fiona, Stevens Angela, Smith Anna, Morris Robin G, Murphy Declan G M, Murphy Kieran C

Abstract excerpt

OBJECTIVE: Velo-cardio-facial syndrome or 22q11.2 deletion syndrome (22q11DS) is the most common known microdeletion syndrome. One of the genes in the deleted region is the catechol-O-methyltransferase (COMT) gene, which is thought to have significant effects on cognition through its influence on dopamine metabolism. The aim of the present study was to better characterize the cognitive phenotype in a large cohort...

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Source

Identifiers

PMID: 20307169
DOI: 10.3109/00048670903489882

Genes

COMT

Provenance

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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COMT and anxiety and cognition in children with chromosome 22q11.2 deletion syndrome.Semantic proximity Read ↗

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