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...
Main Authors: | Maurice J C M Magnée, Victor A F Lamme, Monique G M de Sain-van der Velden, Jacob A S Vorstman, Chantal Kemner |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2011-01-01
|
Series: | PLoS ONE |
Online Access: | http://europepmc.org/articles/PMC3187802?pdf=render |
Similar Items
-
The Genetics and Epigenetics of 22q11.2 Deletion Syndrome
by: Qiumei Du, et al.
Published: (2020-02-01) -
FAMILIAL CASE OF CHROMOSOME 22q11.2 DELETION SYNDROME
by: I. A. Tuzankina, et al.
Published: (2017-01-01) -
Visual processing deficits in 22q11.2 Deletion Syndrome
by: Marjan Biria, et al.
Published: (2018-01-01) -
Hematological abnormalities and 22q11.2 deletion syndrome
by: Rafael Fabiano Machado Rosa, et al.
Published: (2011-01-01) -
The developmental cognitive trajectory of the 22q11.2 deletion
by: Jacobson, Clare Elizabeth Harvey
Published: (2012)