Assessing the association of common genetic variants in EPHB4 and RASA1 with phenotype severity in familial cerebral cavernous malformation.

Mol Genet Genomic Med · 2021 · PMC8580075 · PMID 34491620

Europe PMC DOI

hedged sentence

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closest p

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boldest claim

The sentences

nominally significantno p-value reported

SNPs with a Bonferroni‐adjusted p value ≤0.05 and >0.007 were considered to be nominally significant.

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