Specific differences in temporal binding aspects of the attentional blink in Chromosome 22q11.2 Deletion Syndrome

Chromosome 22q11.2 Deletion Syndrome (22q11DS) is a genetic syndrome characterized by a variety of cognitive impairments, including difficulty with attention. 22q11DS is the strongest known genetic risk factor for developing schizophrenia, a disorder characterized by impairments in visual attention...

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Bibliographic Details
Main Authors: Antshel, K.M (Author), Fremont, W. (Author), Kates, W.R (Author), Kopec, J. (Author), Russo, N. (Author)
Format: Article
Language:English
Published: Masson SpA 2018
Subjects:
age
Online Access:View Fulltext in Publisher