Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD.

Nat Commun · 2023 · PMC10700338 · PMID 38057346

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highly significantno p-value reported

Strikingly, within these regions both Mis3 variants alone as well as LGD + Mis3 variants as a group (i.e., damaging variants) showed highly significant enrichment.

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