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Schizophrenia-like neurophysiological abnormalities in 22q11.2 deletion syndrome and their association to COMT and PRODH genotypes

✍ Scribed by Zarchi, Omer; Carmel, Miri; Avni, Chen; Attias, Josef; Frisch, Amos; Michaelovsky, Elena; Patya, Miriam; Green, Tamar; Weinberger, Ronnie; Weizman, Abraham; Gothelf, Doron

Book ID: 123463761
Publisher: Elsevier Science
Year: 2013
Tongue: English
Weight: 492 KB
Volume: 47
Category: Article
ISSN: 0022-3956
DOI: 10.1016/j.jpsychires.2013.07.004

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