Barely Significant
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The landscape of gene mutations in a cohort of 3353 Han Chinese children with nonsyndromic hearing loss.

EBioMedicine · 2026 · PMC12999288 · PMID 41833579

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highly significantP < 0.0001actually significant
Furthermore, an Area Under the Curve (AUC) analysis ( Figure S4E ) confirmed a highly significant overall hearing deficit in the Foxi1 N155del/+ mice (95% CI = [1254, 1675]; P < 0.0001; t-test).

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