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MAOB variants identified in SCZ individuals. The corresponding family pedigree (the proband is indicated by an arrow) and chromatograms for the proband (P) and control (C), as well as amino-acid conservation, are shown for each variant. (a) Nonsense variant identified during the first screening of 143 SCZ patients. (b) Missense variants identified during the screening of 190 additional SCZ patients.
