Barely Significant
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Computational analysis of splicing errors and mutations in human transcripts.

BMC Genomics · 2008 · PMC2234086 · PMID 18194514

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marginally significantno p-value reported
In retained introns, the most prevalent candidate splicing enhancers were those for SF2/ASF and SC35, trailed by those for SRp40 and, marginally significant, for SRp55.

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