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CORRECTION article

Front. Mol. Neurosci., 01 March 2024
Sec. Molecular Signalling and Pathways

Corrigendum: ATP6V0C is associated with febrile seizures and epilepsy with febrile seizures plus

\r\nYang Tian&#x;Yang Tian1Qiong-Xiang Zhai&#x;Qiong-Xiang Zhai2Xiao-Jing Li&#x;Xiao-Jing Li1Zhen ShiZhen Shi1Chuan-Fang Cheng,Chuan-Fang Cheng3,4Cui-Xia Fan,Cui-Xia Fan3,4Bin Tang,Bin Tang3,4Ying ZhangYing Zhang5Yun-Yan He,Yun-Yan He3,4Wen-Bin Li,Wen-Bin Li3,4Sheng Luo,Sheng Luo3,4Chi HouChi Hou1Wen-Xiong Chen
Wen-Xiong Chen1*Wei-Ping Liao,Wei-Ping Liao3,4Jie Wang,
 for the China Epilepsy Gene . ProjectJie 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
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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, d2FuZ2ppZTIwMTQwMTAmI3gwMDA0MDsxNjMuY29t; Wen-Xiong Chen, Y2hlbndlbnhpb25nJiN4MDAwNDA7Z3djbWMub3Jn

These authors have contributed equally to this work

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