A population genetic approach to mapping neurological disorder genes using deep resequencing.

PLoS Genet · 2011 · PMC3044677 · PMID 21383861

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nominally significantno p-value reported

Like GRIN2B , CACNA1F also shows concordance among methods within the ASD cohort; including a nominally significant missense to silent variant ratio, a significant collapsing method result, and a negative shift in the γ mkprf estimate relative to the control cohort.

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