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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...
Autores principales: | van Duin, Esther D. A., Goossens, Liesbet, Hernaus, Dennis, da Silva Alves, Fabiana, Schmitz, Nicole, Schruers, Koen, van Amelsvoort, Therese |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
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 |
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