Schizophrenia-like neurophysiological abnormalities in 22q11.2 deletion syndrome and their association to COMT and PRODH genotypes. [electronic resource]
Producer: 20140513Description: 1623-9 p. digitalISSN:- 1879-1379
- 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
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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