Transcripts derived from AmnSINE1 repetitive sequences are depleted in the cortex of autism spectrum disorder patients.

Front Bioinform · 2025 · PMC12015672 · PMID 40270680

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highly significantno p-value reported

The intersection between AmnSINE1-containing loci and SFARI genes was highly significant, highlighting that AmnSINE1-containing loci and genes implicated in autism susceptibility were not randomly interlaced.

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