ArticleJournal of clinical immunology2024

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.

Aimee Huynh et al.PubMed ↗Full text ↗Publisher ↗

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