Barely Significant
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The Frog <i>Xenopus</i> as a Model to Study Joubert Syndrome: The Case of a Human Patient With Compound Heterozygous Variants in <i>PIBF1</i>.

Front Physiol · 2019 · PMC6397843 · PMID 30858804

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highly significantno p-value reported
As shown in Figures 6E–G , the WT human gene rescued cilia numbers in a highly significant manner.

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