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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Detalles Bibliográficos
Autores principales: van Duin, Esther D. A., Goossens, Liesbet, Hernaus, Dennis, da Silva Alves, Fabiana, Schmitz, Nicole, Schruers, Koen, van Amelsvoort, Therese
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4946156/
https://www.ncbi.nlm.nih.gov/pubmed/27429661
http://dx.doi.org/10.1186/s11689-016-9158-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4946156/
https://www.ncbi.nlm.nih.gov/pubmed/27429661
http://dx.doi.org/10.1186/s11689-016-9158-5

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