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 Huynh¹, Paul E Gray^{2

3

4}, Anna Sullivan^{1

2}, Joseph Mackie^{5

6}, Antoine Guerin^{5

6}, Geetha Rao⁵, Karrnan Pathmanandavel^{5

6}, Erika Della Mina^{5

6}, Georgina Hollway^{2

5}, Matthew Hobbs⁵, Karen Enthoven^{2

5}, Patrick O'Young^{2

5}, Sam McManus⁷, Luke H Wainwright⁷, Megan Higgins⁸, Fallon Noon⁸, Melanie Wong^{2

9}, Paul Bastard^{10

11

12

13}, Qian Zhang¹¹, Jean-Laurent Casanova^{10

11

12

13

14}, Kuang-Chih Hsiao^{2

15

16}, Alberto Pinzon-Charry^{1

2

17}, Cindy S Ma^{2

5

6}, Stuart G Tangye^{18

19

20}

Affiliations

¹ Queensland Paediatric Immunology and Allergy Service, Children's Health Queensland, Brisbane, QLD 4101, Australia.
² Clinical Immunogenomics Research Consortium, Australasia, Australia.
³ School Medicine, Western Sydney University, Penrith, NSW, Australia.
⁴ Department of Immunology and Infectious Diseases, Sydney Children's Hospital, Randwick, Australia.
⁵ Garvan Institute of Medical Research, 384 Victoria St, Darlinghurst, NSW, 2010, Australia.
⁶ School of Clinical Medicine, Faculty of Medicine and Health, UNSW Sydney, Sydney, NSW, Australia.
⁷ Royal Brisbane and Women's Hospital, Herston, QLD, Australia.
⁸ Genetic Health Queensland, Brisbane, Australia.
⁹ Department of Allergy and Immunology, The Children's Hospital at Westmead, Sydney, NSW, Australia.
¹⁰ Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM U1163, Necker Hospital for Sick Children, Paris, France.
¹¹ St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, NY, USA.
¹² University of Paris, Imagine Institute, Paris, France.
¹³ Department of Pediatrics, Necker Hospital for Sick Children, AP-HP, Paris, France.
¹⁴ Howard Hughes Medical Institute, New York, USA.
¹⁵ Starship Child Health, Auckland, New Zealand.
¹⁶ Department of Paediatrics, University of Auckland, Auckland, New Zealand.
¹⁷ Griffith University and University, Queensland, Australia.
¹⁸ Clinical Immunogenomics Research Consortium, Australasia, Australia. s.tangye@garvan.org.au.
¹⁹ Garvan Institute of Medical Research, 384 Victoria St, Darlinghurst, NSW, 2010, Australia. s.tangye@garvan.org.au.
²⁰ School of Clinical Medicine, Faculty of Medicine and Health, UNSW Sydney, Sydney, NSW, Australia. s.tangye@garvan.org.au.

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

Published Erratum

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. J Clin Immunol. 2024.

. 2024 Sep 19;45(1):11.

doi: 10.1007/s10875-024-01801-x.

Authors

Affiliations

¹ Queensland Paediatric Immunology and Allergy Service, Children's Health Queensland, Brisbane, QLD 4101, Australia.
² Clinical Immunogenomics Research Consortium, Australasia, Australia.
³ School Medicine, Western Sydney University, Penrith, NSW, Australia.
⁴ Department of Immunology and Infectious Diseases, Sydney Children's Hospital, Randwick, Australia.
⁵ Garvan Institute of Medical Research, 384 Victoria St, Darlinghurst, NSW, 2010, Australia.
⁶ School of Clinical Medicine, Faculty of Medicine and Health, UNSW Sydney, Sydney, NSW, Australia.
⁷ Royal Brisbane and Women's Hospital, Herston, QLD, Australia.
⁸ Genetic Health Queensland, Brisbane, Australia.
⁹ Department of Allergy and Immunology, The Children's Hospital at Westmead, Sydney, NSW, Australia.
¹⁰ Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM U1163, Necker Hospital for Sick Children, Paris, France.
¹¹ St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, NY, USA.
¹² University of Paris, Imagine Institute, Paris, France.
¹³ Department of Pediatrics, Necker Hospital for Sick Children, AP-HP, Paris, France.
¹⁴ Howard Hughes Medical Institute, New York, USA.
¹⁵ Starship Child Health, Auckland, New Zealand.
¹⁶ Department of Paediatrics, University of Auckland, Auckland, New Zealand.
¹⁷ Griffith University and University, Queensland, Australia.
¹⁸ Clinical Immunogenomics Research Consortium, Australasia, Australia. s.tangye@garvan.org.au.
¹⁹ Garvan Institute of Medical Research, 384 Victoria St, Darlinghurst, NSW, 2010, Australia. s.tangye@garvan.org.au.
²⁰ School of Clinical Medicine, Faculty of Medicine and Health, UNSW Sydney, Sydney, NSW, Australia. s.tangye@garvan.org.au.

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

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Erratum for

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.
Huynh A, Gray PE, Sullivan A, Mackie J, Guerin A, Rao G, Pathmanandavel K, Mina ED, Hollway G, Hobbs M, Enthoven K, O'Young P, McManus S, Wainwright LH, Higgins M, Noon F, Wong M, Bastard P, Zhang Q, Casanova JL, Hsiao KC, Pinzon-Charry A, Ma CS, Tangye SG. Huynh A, et al. J Clin Immunol. 2024 Aug 5;44(8):170. doi: 10.1007/s10875-024-01774-x. J Clin Immunol. 2024. PMID: 39098944 Free PMC article.

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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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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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