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

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J Clin Immunol. 2024 Sep 19;45(1):11. doi: 10.1007/s10875-024-01801-x.

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PMID:39297999 | PMC:PMC11413082 | DOI:10.1007/s10875-024-01801-x

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