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Genotypic and Haplotypic Association of Catechol-<i>O</i>-Methyltransferase rs4680 and rs4818 Gene Polymorphisms with Particular Clinical Symptoms in Schizophrenia.

Genes (Basel) · 2023 · PMC10379812 · PMID 37510262

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Additionally, nominal association of COMT rs4818 polymorphism and scores on G1 item (corresponding to the intensity of somatic concern) was observed, where G allele was under-represented (19.3%) in male subjects with mild symptoms (R = −1.4; χ 2 = 4.186; p = 0.041) compared to C allele carriers (24.7%); however, after correction for multiple testing, this association did not reach statistical significance.

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