In the published article, there was an error in Affiliation [1]. Instead of “Department of Pediatrics, West China Second University Hospital, Chengdu, Sichuan, China,” it should be “Department of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.”
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.
Statements
Publisher’s note
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Summary
Keywords
autosomal recessive cutis laxa type 1B, ARCL1B, EFEMP2, heart failure, arterial dysplasia
Citation
Ouyang L, Yang F, Duan H and Wang C (2025) Corrigendum: Case report and literature review: delayed diagnosis of ARCL1B due to a newly reported homozygous mutation c.464A>C p. (Tyr155Ser) in the EFEMP2 gene. Front. Genet. 16:1589037. doi: 10.3389/fgene.2025.1589037
Received
06 March 2025
Accepted
07 March 2025
Published
13 March 2025
Approved by
Frontiers Editorial Office, Frontiers Media SA, Switzerland
Volume
16 - 2025
Updates
Copyright
© 2025 Ouyang, Yang, Duan 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: Chuan Wang, wangchuan1308@163.com; Hongyu Duan, 495429978@qq.com
†These authors have contributed equally to this work
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.