Barely Significant
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Exome sequencing in families with chronic central serous chorioretinopathy.

Mol Genet Genomic Med · 2019 · PMC6465660 · PMID 30724488

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showed a trendno p-value reported
Of the five genes nominally associated in the case–control cohort, the DPH1 [OMIM:603527], KIAA1324 [OMIM:611298], and PREX1 [OMIM:606905] genes showed a trend toward association in the family dataset and might be interesting genes for replication in a larger CSC cohorts.

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