Barely Significant
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A sex-specific association of common variants of neuroligin genes (NLGN3 and NLGN4X) with autism spectrum disorders in a Chinese Han cohort.

Behav Brain Funct · 2011 · PMC3120659 · PMID 21569590

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nominally significantno p-value reported
As shown in Table 2 , nominally significant differences of allele frequencies were detected for three SNPs in NLGN3 gene in total samples contrasted between individuals with ASDs and controls and these differences remained significant after Bonferroni correction for multiple testing.

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