Front. Genet. Frontiers in Genetics Front. Genet. 1664-8021 Frontiers Media S.A. 1620297 10.3389/fgene.2025.1620297 Genetics Correction Corrigendum: Corrigendum: Application of rapid clinical exome sequencing technology in the diagnosis of critically ill pediatric patients with suspected genetic diseases Ouyang et al. 10.3389/fgene.2025.1620297 Ouyang Xuejun 1 † Chi Dazhi 2 † Zhang Yu 1 Yu Tian 3 Zhang Qian 4 Xu Lei 4 Zhang Victor Wei 4 Wang Bin 1 * 1 The Neonatal Intensive Care Unit, Zhujiang Hospital, Southern Medical University, Guangzhou, Guangdong, China 2 Department of Emergency, Zhujiang Hospital, Southern Medical University, Guangzhou, Guangdong, China 3 The Pediatric Intensive Care Unit, Hunan Provincial People’s Hospital, Changsha, Hunan, China 4 Department of Genomic Medicine, AmCare Genomics Lab, Guangzhou, Guangdong, China

Approved by: Frontiers Editorial Office, Frontiers Media SA, Switzerland

 *Correspondence: Bin Wang, gzwangbin@smu.edu.cn

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

 12 05 2025 2025 16 1620297 29 04 2025 30 04 2025 Copyright © 2025 Ouyang, Chi, Zhang, Yu, Zhang, Xu, Zhang and Wang. 2025 Ouyang, Chi, Zhang, Yu, Zhang, Xu, Zhang and Wang

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 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 clinical exome sequencing mtDNA sequencing critical illness rapid genetic diagnosis pediatric section-at-acceptance Genetics of Common and Rare Diseases

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.

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