Whole Exome Sequencing of Patients from Multicase Families with Systemic Lupus Erythematosus Identifies Multiple Rare Variants.

Of note, when including mouse phenotype data in the analysis, we observed highly significant enrichment of a phenotype of absent immature B cells ( DCLRE1C , p (FDR-corrected) = 5.3 × 10 −6 ).

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