Prognostic Value of Genotype-Phenotype Correlations in X-Linked Myotubular Myopathy and the Use of the Face2Gene Application as an Effective Non-Invasive Diagnostic Tool.

Genes (Basel) · 2023 · PMC10742680 · PMID 38136996

Europe PMC DOI

hedged sentence

0.0010

closest p · 0.0× alpha

0.0010

boldest claim

The sentences

highly significantp < 0.001actually significant

We found that 95.2% of all truncating variants were associated with severe phenotype; this association was highly significant ( p < 0.001).

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