Barely Significant
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Diverse monogenic subforms of human spermatogenic failure.

Nat Commun · 2022 · PMC9792524 · PMID 36572685

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nominally significantno p-value reported
Burden testing identified 21 genes with nominally significant p -values, providing further evidence that variation in these genes is likely deleterious for human male infertility (Supplementary Table 4 ).

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