TY  - GEN
AU  - Zarchi,Omer
AU  - Carmel,Miri
AU  - Avni,Chen
AU  - Attias,Josef
AU  - Frisch,Amos
AU  - Michaelovsky,Elena
AU  - Patya,Miriam
AU  - Green,Tamar
AU  - Weinberger,Ronnie
AU  - Weizman,Abraham
AU  - Gothelf,Doron
TI  - Schizophrenia-like neurophysiological abnormalities in 22q11.2 deletion syndrome and their association to COMT and PRODH genotypes
SN  - 1879-1379
PY  - 2014///0513
KW  - 22q11 Deletion Syndrome
KW  - genetics
KW  - Acoustic Stimulation
KW  - Adolescent
KW  - Adult
KW  - Catechol O-Methyltransferase
KW  - Child
KW  - Contingent Negative Variation
KW  - Endophenotypes
KW  - Female
KW  - Genetic Association Studies
KW  - Genetic Predisposition to Disease
KW  - Genotype
KW  - Humans
KW  - Male
KW  - Polymorphism, Single Nucleotide
KW  - Proline Oxidase
KW  - Schizophrenia
KW  - physiopathology
KW  - Sensory Gating
KW  - Young Adult
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1016/j.jpsychires.2013.07.004
ER  -