CORRECTION article

Front. Genet., 12 May 2025

Sec. Genetics of Common and Rare Diseases

Volume 16 - 2025 | https://doi.org/10.3389/fgene.2025.1620297

Corrigendum: Corrigendum: Application of rapid clinical exome sequencing technology in the diagnosis of critically ill pediatric patients with suspected genetic diseases

This article is a correction to:

  1. Application of rapid clinical exome sequencing technology in the diagnosis of critically ill pediatric patients with suspected genetic diseases

    1. Read original article
Xuejun Ouyang&#x;Xuejun Ouyang1†Dazhi Chi&#x;Dazhi Chi2†Yu ZhangYu Zhang1Tian YuTian Yu3Qian ZhangQian Zhang4Lei XuLei Xu4Victor Wei ZhangVictor Wei Zhang4Bin Wang Bin Wang1*
  • 1The Neonatal Intensive Care Unit, Zhujiang Hospital, Southern Medical University, Guangzhou, Guangdong, China
  • 2Department of Emergency, Zhujiang Hospital, Southern Medical University, Guangzhou, Guangdong, China
  • 3The Pediatric Intensive Care Unit, Hunan Provincial People’s Hospital, Changsha, Hunan, China
  • 4Department of Genomic Medicine, AmCare Genomics Lab, Guangzhou, Guangdong, China

A Corrigendum on
Corrigendum: Application of rapid clinical exome sequencing technology in the diagnosis of critically ill pediatric patients with suspected genetic diseases

by Ouyang X, Chi D, Zhang Y, Yu T, Zhang Q, Xu L, Zhang VW and Wang B (2025). Front. Genet. 16:1592212. doi: 10.3389/fgene.2025.1592212

In the published article, it was erroneously excluded that Authors Xuejun Ouyang and Dazhi Chi contributed equally to the work and share first authorship.

The authors apologize for this error 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: clinical exome sequencing, mtDNA sequencing, critical illness, rapid genetic diagnosis, pediatric

Citation: Ouyang X, Chi D, Zhang Y, Yu T, Zhang Q, Xu L, Zhang VW and Wang B (2025) Corrigendum: Corrigendum: Application of rapid clinical exome sequencing technology in the diagnosis of critically ill pediatric patients with suspected genetic diseases. Front. Genet. 16:1620297. doi: 10.3389/fgene.2025.1620297

Received: 29 April 2025; Accepted: 30 April 2025;
Published: 12 May 2025.

Approved by:

Frontiers Editorial Office, Frontiers Media SA, Switzerland

Copyright © 2025 Ouyang, Chi, Zhang, Yu, Zhang, Xu, Zhang and Wang. 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: Bin Wang, Z3p3YW5nYmluQHNtdS5lZHUuY24=

†These authors have contributed equally to this work and share first authorship

Disclaimer: 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.