Neural correlates of reward processing in adults with 22q11 deletion syndrome

BACKGROUND: 22q11.2 deletion syndrome (22q11DS) is caused by a microdeletion on chromosome 22q11.2 and associated with an increased risk to develop psychosis. The gene coding for catechol-O-methyl-transferase (COMT) is located at the deleted region, resulting in disrupted dopaminergic neurotransmiss...

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Bibliografiska uppgifter
I publikationen:J Neurodev Disord
Huvudupphovsmän: van Duin, Esther D. A., Goossens, Liesbet, Hernaus, Dennis, da Silva Alves, Fabiana, Schmitz, Nicole, Schruers, Koen, van Amelsvoort, Therese
Materialtyp: Artigo
Språk:Inglês
Publicerad: BioMed Central 2016
Ämnen:
Research
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC4946156/
https://ncbi.nlm.nih.gov/pubmed/27429661
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s11689-016-9158-5
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