Identification of rare X-linked neuroligin variants by massively parallel sequencing in males with autism spectrum disorder.

Mol Autism · 2012 · PMC3492087 · PMID 23020841

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hedged sentence

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closest p · 2.0× alpha

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boldest claim

The sentences

showed a trendP < 0.10so close (0.05 < p ≤ 0.1)

The construct bearing the 3’UTR NLGN3 variant (chrX:70306922) showed a trend for reduced luciferase activity the Neuro2a ( P < 0.10) cells compared to the construct with the reference sequence (see Additional file 8 ).

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