This article is a correction to:
Functional Studies of Novel FOXL2 Variants in Chinese Families With Blepharophimosis–Ptosis–Epicanthus Inversus Syndrome
Mingyu Zhao
Xiaolu Meng2- 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, ChinaCopyright © 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, wtlcom@sina.com