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CORRECTION article

Front. Genet., 29 April 2024
Sec. Genetics of Common and Rare Diseases

Corrigendum: Novel FOXL2 variants in two Chinese families with blepharophimosis, ptosis, and epicanthus inversus syndrome

Mingyu ZhaoMingyu Zhao1Xiaolu MengXiaolu Meng2Jiaqi WangJiaqi Wang1Tailing Wang
Tailing Wang1*
  • 1The Department of Facial and Neck Plastic Surgery, Plastic Surgery Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China
  • 2Plastic Surgery Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China

A Corrigendum on
Novel FOXL2 variants in two Chinese families with blepharophimosis, ptosis, and epicanthus inversus syndrome

by Zhao M, Meng X, Wang J and Wang T (2024). Front. Genet. 15:1343411. doi: 10.3389/fgene.2024.1343411

In the published article, there was an error in the legend for Figure 3 as published. The text of the legend for Figure 3 is written backwards: “Protein expression and distribution. Subcellular localization of EGFP, FOXL2, FOXL2-MT1, and FOXL2-MT2. The first column shows the nuclei stained with Hoechst33342; the second column shows the subcellular localization of EGFP or FOXL2 as an EGFP-tagged fusion protein. The third column shows the combined images of the above images (400× magnification).”

The contents of the first and second columns should be exchanged. The corrected legend should read as “The first column shows the subcellular localisation of EGFP as a marker for FOXL2 protein; the second column shows the nuclei stained with Hoechst33342.”

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: blepharophimosis-ptosis-epicanthus inversus syndrome, FOXL2 variant, whole exome sequencing, tansfection, protein model prediction

Citation: Zhao M, Meng X, Wang J and Wang T (2024) Corrigendum: Novel FOXL2 variants in two Chinese families with blepharophimosis, ptosis, and epicanthus inversus syndrome. Front. Genet. 15:1414939. doi: 10.3389/fgene.2024.1414939

Received: 09 April 2024; Accepted: 15 April 2024;
Published: 29 April 2024.

Edited and reviewed by:

Yongchu Pan, Nanjing Medical University, China

Copyright © 2024 Zhao, Meng, Wang 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: Tailing Wang, d3RsY29tQHNpbmEuY29t

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.