Yang Tian1†
Qiong-Xiang Zhai2†
Xiao-Jing Li1†
Zhen Shi1
Chuan-Fang Cheng3,4
Cui-Xia Fan3,4
Bin Tang3,4Ying Zhang5Yun-Yan He3,4
Wen-Bin Li3,4
Sheng Luo3,4
Chi Hou1
Wen-Xiong Chen1*
Wei-Ping Liao3,4
Jie Wang3,4* for the China Epilepsy Gene 1.0 Project- 1Department of Neurology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China
- 2Department of Pediatrics, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China
- 3Department of Neurology, Institute of Neuroscience, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China
- 4Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province, Ministry of Education of China, Guangzhou, China
- 5The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, China
A corrigendum on
ATP6V0C is associated with febrile seizures and epilepsy with febrile seizures plus
by Tian, Y., Zhai, Q.-X., Li, X.-J., Shi, Z., Cheng, C.-F., Fan, C.-X., Tang, B., Zhang, Y., He, Y.-Y., Li, W.-B., Luo, S., Hou, C., Chen, W.-X., Liao, W.-P., and Wang, J. (2022). Front. Mol. Neurosci. 15:889534. doi: 10.3389/fnmol.2022.889534
In the published article, there was an error in Panel B of Figure 1 as published. On the Case 2 pedigree, the mother's and father's chromatograms have been reversed. The corrected Figure 1 and its caption “Figure 1 | Genetic data of cases with ATP6V0C mutations. ” appear below.
Figure 1. Genetic data of cases with ATP6V0C mutations. (A) Pedigrees of the two families with ATP6V0C mutations and their corresponding phenotypes. Individuals with mutation are marked as m/+, and those without mutation are marked as +/+. (B) DNA sequencing chromatograms of the two families with ATP6V0C mutations. Red arrows indicate the positions of the mutations. (C) Amino acid sequence alignment of the missense mutation shows that residue Ala22 is highly conserved in various species.
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: ATP6V0C, loss of function, febrile seizures, epilepsy with febrile seizures plus, whole-exome sequencing
Citation: Tian Y, Zhai Q-X, Li X-J, Shi Z, Cheng C-F, Fan C-X, Tang B, Zhang Y, He Y-Y, Li W-B, Luo S, Hou C, Chen W-X, Liao W-P and Wang J (2024) Corrigendum: ATP6V0C is associated with febrile seizures and epilepsy with febrile seizures plus. Front. Mol. Neurosci. 17:1385915. doi: 10.3389/fnmol.2024.1385915
Received: 14 February 2024; Accepted: 19 February 2024;
Published: 01 March 2024.
Edited and reviewed by: Rossella Di Giaimo, University of Naples Federico II, Italy
Copyright © 2024 Tian, Zhai, Li, Shi, Cheng, Fan, Tang, Zhang, He, Li, Luo, Hou, Chen, Liao 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: Jie Wang, wangjie2014010@163.com; Wen-Xiong Chen, chenwenxiong@gwcmc.org
†These authors have contributed equally to this work