Familial Atrial Septal Defect and Sudden Cardiac Death: Identification of a Novel NKX2-5 Mutation and a Review of the Literature.

Congenit Heart Dis · 2016 · PMC5019245 · PMID 26679770

Europe PMC DOI

hedged sentence

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closest p · 0.0× alpha

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boldest claim

The sentences

highly significantP = 7.1 × 10 −9actually significant

We found a highly significant increased frequency of mutations in familial cases compared to nonfamilial cases ( P = 7.1 × 10 −9 ).

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