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

Spread the love

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

NO ABSTRACT

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

Leave a Comment

deneme bonusu veren siteler - canlı bahis siteleri - casino siteleri casino siteleri deneme bonusu veren siteler canlı casino siteleri news news news news news news news news news news news news news news news news news news news news news news news news news news news news news news news news news news news news news news news news news news news news news news news news news news news news news news