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Correction to: A Novel Case of IFNAR1 Deficiency Identified a Common Canonical Splice Site Variant in DOCK8 in Western Polynesia: The Importance of Validating Variants of Unknown Significance in Under-Represented Ancestries

Crossref DOI link: https://doi.org/10.1007/s10875-024-01801-x

Published Online: 2024-09-19

Published Print: 2025-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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