Schizophrenia-like neurophysiological abnormalities in 22q11.2 deletion syndrome and their association to COMT and PRODH genotypes.
Zarchi, Omer
Schizophrenia-like neurophysiological abnormalities in 22q11.2 deletion syndrome and their association to COMT and PRODH genotypes. [electronic resource] - Journal of psychiatric research Nov 2013 - 1623-9 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1879-1379
10.1016/j.jpsychires.2013.07.004 doi
22q11 Deletion Syndrome--genetics
Acoustic Stimulation
Adolescent
Adult
Catechol O-Methyltransferase--genetics
Child
Contingent Negative Variation--genetics
Endophenotypes
Female
Genetic Association Studies
Genetic Predisposition to Disease
Genotype
Humans
Male
Polymorphism, Single Nucleotide--genetics
Proline Oxidase--genetics
Schizophrenia--physiopathology
Sensory Gating--genetics
Young Adult
Schizophrenia-like neurophysiological abnormalities in 22q11.2 deletion syndrome and their association to COMT and PRODH genotypes. [electronic resource] - Journal of psychiatric research Nov 2013 - 1623-9 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1879-1379
10.1016/j.jpsychires.2013.07.004 doi
22q11 Deletion Syndrome--genetics
Acoustic Stimulation
Adolescent
Adult
Catechol O-Methyltransferase--genetics
Child
Contingent Negative Variation--genetics
Endophenotypes
Female
Genetic Association Studies
Genetic Predisposition to Disease
Genotype
Humans
Male
Polymorphism, Single Nucleotide--genetics
Proline Oxidase--genetics
Schizophrenia--physiopathology
Sensory Gating--genetics
Young Adult