94% of researchers rate our articles as excellent or good
Learn more about the work of our research integrity team to safeguard the quality of each article we publish.
Find out more
CORRECTION article
Front. Genet.
Sec. Genetics of Common and Rare Diseases
Volume 16 - 2025 | doi: 10.3389/fgene.2025.1589037
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
Provisionally accepted- 1 West China Second University Hospital, Sichuan University, Chengdu, China
- 2 Key Laboratory of Birth Defects and Related Diseases of Women and Children, West China Second University Hospital, Sichuan University, Chengdu, Sichuan Province, China
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 Affiliations of all authors as they appear in the published original version of the article 1Department of Pediatrics, West China Second University Hospital, Sichuan University, 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* Correspondence: wangchuan1308@163.comKeywords: autosomal recessive cutis laxa type 1B, ARCL1B, EFEMP2, heart failure, arterial dysplasia Corrigendum on: Ouyang L, Yang F, Duan H and Wang C (2024) 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. 15:1453195. doi: 10.3389/fgene.2024.1453195 Incorrect AffiliationIn 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.
Keywords: Autosomal recessive cutis laxa type 1B, ARCL1B, EFEMP2, Heart Failure, arterial dysplasia
Received: 06 Mar 2025; Accepted: 07 Mar 2025.
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) or licensor 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:
Hongyu Duan, West China Second University Hospital, Sichuan University, Chengdu, China
Chuan Wang, West China Second University Hospital, Sichuan University, Chengdu, China
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.