This article is a correction to:
Genetic diagnosis of inborn errors of immunity using clinical exome sequencing
Soon Sung Kwon1
Youn Keong Cho1
Seungmin Hahn2
Jiyoung Oh3
Dongju Won1
Saeam Shin1*
Ji-Man Kang4,5*
Jong Gyun Ahn4,5
Seung-Tae Lee1,6
Jong Rak Choi1,6- 1Department of Laboratory Medicine, Yonsei University College of Medicine, Seoul, Republic of Korea
- 2Department of Pediatric Hemato-oncology, Yonsei Cancer Center, Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea
- 3Division of Clinical Genetics, Department of Pediatrics, Severance Children’s Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea
- 4Department of Pediatrics, Severance Children’s Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea
- 5Institute for Immunology and Immunological Diseases, Yonsei University College of Medicine, Seoul, Republic of Korea
- 6Dxome, Seoul, Republic of Korea
A corrigendum on
Genetic diagnosis of inborn errors of immunity using clinical exome sequencing
by Kwon SS, Cho YK, Hahn S, Oh J, Won D, Shin S, Kang J-M, Ahn JG, Lee S-T and Choi JR (2023). Front. Immunol. 14:1178582. doi: 10.3389/fimmu.2023.1178582
In the published article, there was an error regarding the affiliation for Seung-Tae Lee and Jong Rak Choi. As well as having affiliation 1, they should also have Dxome, Seoul, Republic of Korea.
In the published article, there was an error. In Materials and Methods, the manufacturer of our custom panel was missed.
A correction has been made to Materials and Methods, “Genetic analysis and variant interpretation”, paragraph 1. This sentence previously stated:
“For the genetic diagnosis of IEI, we used a custom-designed clinical exome panel including 4,894 genes related to human genetic diseases, including IEI (Supplementary Table S1).”
The corrected sentence appears below:
“For the genetic diagnosis of IEI, we used a custom-designed clinical exome panel (Dxome, Seoul, Republic of Korea) including 4,894 genes related to human genetic diseases, including IEI (Supplementary Table S1).”
Conflict of interest
Authors S-TL and JC were employed by company Dxome.
The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
The authors apologize for these errors and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Keywords: inborn errors of immunity, next generation sequencing, clinical exome sequencing, genetic diagnosis, somatic variant, incidental finding
Citation: Kwon SS, Cho YK, Hahn S, Oh J, Won D, Shin S, Kang J-M, Ahn JG, Lee S-T and Choi JR (2023) Corrigendum: Genetic diagnosis of inborn errors of immunity using clinical exome sequencing. Front. Immunol. 14:1235318. doi: 10.3389/fimmu.2023.1235318
Received: 06 June 2023; Accepted: 07 June 2023;
Published: 19 June 2023.
Approved by:
Frontiers Editorial Office, Frontiers Media SA, SwitzerlandCopyright © 2023 Kwon, Cho, Hahn, Oh, Won, Shin, Kang, Ahn, Lee and Choi. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Saeam Shin, c2FlYW0wMzA0QHl1aHMuYWM=; Ji-Man Kang, dW1pODdjQHl1aHMuYWM=