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Reduced NoGo-anteriorisation during continuous performance test in deletion syndrome 22q11.2

✍ Scribed by Marcel Romanos; Ann-Christine Ehlis; Christina G. Baehne; Christian Jacob; Tobias J. Renner; Astrid Storch; Wolfgang Briegel; Susanne Walitza; Klaus-Peter Lesch; Andreas J. Fallgatter


Book ID
113750648
Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
938 KB
Volume
44
Category
Article
ISSN
0022-3956

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## Abstract 22q11.2 deletion syndrome (22q11.2DS) is a well‐known genetic risk factor for schizophrenia. The catechol‐__O__‐methyltransferase (COMT) gene falls within the 22q11.2 minimal critical region of the deletion. Brain activity, as measured by functional magnetic resonance imaging (fMRI) dur