Barely Significant
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Microtubule modification defects underlie cilium degeneration in cell models of retinitis pigmentosa associated with pre-mRNA splicing factor mutations.

Front Genet · 2022 · PMC9513239 · PMID 36176300

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highly significantno p-value reported
Exon skipping in multiple transcripts of TTLL3 was highly significant in PRPF6 +/c.2185C>T mutants.

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