A common variant in myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults.

Transl Psychiatry · 2013 · PMC3591001 · PMID 23423138

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hedged sentence

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closest p

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boldest claim

The sentences

nominally significantno p-value reported

The SNP rs13058434 (p.P177L) showed nominally significant association with BMAF in the subgroup of children who were not-at-risk according to rs133885 genotype.

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