Proline and COMT Status Affect Visual Connectivity in Children with 22q11.2 Deletion Syndrome

BACKGROUND: Individuals with the 22q11.2 deletion syndrome (22q11DS) are at increased risk for schizophrenia and Autism Spectrum Disorders (ASDs). Given the prevalence of visual processing deficits in these three disorders, a causal relationship between genes in the deleted region of chromosome 22 a...

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Detalhes bibliográficos
Main Authors: Magnée, Maurice J. C. M., Lamme, Victor A. F., de Sain-van der Velden, Monique G. M., Vorstman, Jacob A. S., Kemner, Chantal
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2011
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Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3187802/
https://ncbi.nlm.nih.gov/pubmed/21998713
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0025882
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