Clinical and genetic characterization of NIPA1 mutations in a Taiwanese cohort with hereditary spastic paraplegia.

Ann Clin Transl Neurol · 2023 · PMC10014004 · PMID 36607129

Europe PMC DOI

hedged sentence

0.0517

closest p · 1.0× alpha

0.0517

boldest claim

The sentences

close to the boundary of significanceP = 0.0517so close (0.05 < p ≤ 0.1)

There was no significant difference between the wild‐type protein and the c.316G>C NIPA1, although the P value was close to the boundary of significance ( P = 0.0517).

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