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
更正:西波利尼西亚一例新型 IFNAR1 缺陷病例揭示 DOCK8 中常见的典型剪接位点变异:验证代表性不足的祖先中意义不明的变异的重要性
期刊:Journal of Clinical Immunology
影响因子:5.7
doi:10.1007/s10875-024-01801-x
Huynh, Aimee; E Gray, Paul; Sullivan, Anna; Mackie, Joseph; Guerin, Antoine; Rao, Geetha; Pathmanandavel, Karrnan; Della Mina, Erika; Hollway, Georgina; Hobbs, Matthew; Enthoven, Karen; O'Young, Patrick; McManus, Sam; H Wainwright, Luke; Higgins, Megan; Noon, Fallon; Wong, Melanie; Bastard, Paul; Zhang, Qian; Casanova, Jean-Laurent; Hsiao, Kuang-Chih; Pinzon-Charry, Alberto; S Ma, Cindy; G Tangye, Stuart