Barely Significant
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AON-Mediated Exon Skipping to Bypass Protein Truncation in Retinal Dystrophies Due to the Recurrent <i>CEP290</i> c.4723A > T Mutation. Fact or Fiction?

Genes (Basel) · 2019 · PMC6562928 · PMID 31091803

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highly significantno p-value reported
The same treatment in P1 cells, allowed a highly significant increase in CEP290 ∆36aa protein abundance, as determined by western blot and immunocytochemistry analyses ( Figure 9 A–C).

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