Phenotypically distinct subtypes of psychosis accompany novel or rare variants in four different signaling genes.

Multiple separate ANCOVA analyses comparing each mutation carrier group to the non-carriers, adjusting for sex, age, and age of onset showed SLC39A13 had higher scores for general psychopathology (F[1,27] = 10 ∙ 45, p = .003) and activation (F[1,27] = 8.79, p = .006) meeting the studies Bonferroni corrected significance level of < .01, with other consistent but only marginally significant results for autism (F[1,27] = 6.17, p = .02), PANSS negative scale scores (F[1,27] = 5.28, p = .03) and negative factor scores (F[1,27] = 5.52, p = .026).

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