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
Titel:
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
Auteur:
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