Nationwide Characterization of MFN2-Related CMT in 176 Japanese Patients: Clinical and Genetic Insights.

Ann Clin Transl Neurol · 2026 · PMC12790173 · PMID 41030121

Europe PMC DOI

hedged sentence

0.0990

closest p · 2.0× alpha

0.0990

boldest claim

The sentences

did not reach statistical significancep = 0.099so close (0.05 < p ≤ 0.1)

Although this association did not reach statistical significance (Kruskal–Wallis, p = 0.099), it nonetheless suggests a modulatory role of variant location on disease severity and progression.

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