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...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
Masson SpA
2018
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Subjects: | |
Online Access: | View Fulltext in Publisher |