PMC:4182838 / 162-945 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/PMC/sourceid/4182838","sourcedb":"PMC","sourceid":"4182838","source_url":"http://www.ncbi.nlm.nih.gov/pmc/4182838","text":"Background\n22q11.2 deletion syndrome (22q11DS) is associated with a number of physical anomalies and neuropsychological deficits including impairments in executive and sensorimotor function. It is estimated that 25% of children with 22q11DS will develop schizophrenia and other psychotic disorders later in life. Evidence of genetic transmission of information processing deficits in schizophrenia suggests performance in 22q11DS individuals will enhance understanding of the neurobiological and genetic substrates associated with information processing. In this report, we examine information processing in 22q11DS using measures of startle eyeblink modification and antisaccade inhibition to explore similarities with schizophrenia and associations with neurocognitive performance.","divisions":[{"label":"Title","span":{"begin":0,"end":10}}],"tracks":[{"project":"NEUROSES","denotations":[{"id":"T21","span":{"begin":181,"end":189},"obj":"PATO_0000173"}],"attributes":[{"subj":"T21","pred":"source","obj":"NEUROSES"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"NEUROSES","color":"#93ecad","default":true}]}]}}