CORRECTION article

Front. Genet., 13 March 2025

Sec. Genetics of Common and Rare Diseases

Volume 16 - 2025 | https://doi.org/10.3389/fgene.2025.1589037

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

This article is a correction to:

  1. 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

    1. Read original article
Lixue Ouyang,,Lixue Ouyang1,2,3Fan Yang,Fan Yang1,2Hongyu Duan, &#x;Hongyu Duan1,2*†Chuan Wang,, &#x;Chuan Wang1,2,3*†
  • 1Department of Pediatrics, West China Second University Hospital, Chengdu, Sichuan, China
  • 2Key Laboratory of Birth Defects and Related Diseases of Women and Children, Ministry of Education, Chengdu, China
  • 3Key Laboratory of Development and Diseases of Women and Children of Sichuan Province, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China

A Corrigendum on
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

by Ouyang L, Yang F, Duan H and Wang C (2024). Front. Genet. 15:1453195. doi: 10.3389/fgene.2024.1453195

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.

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: 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

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, d2FuZ2NodWFuMTMwOEAxNjMuY29t; Hongyu Duan, NDk1NDI5OTc4QHFxLmNvbQ==

†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.