Front. Mol. Neurosci. Frontiers in Molecular Neuroscience Front. Mol. Neurosci. 1662-5099 Frontiers Media S.A. 10.3389/fnmol.2024.1385915 Molecular Neuroscience Correction Corrigendum: ATP6V0C is associated with febrile seizures and epilepsy with febrile seizures plus Tian Yang 1 † Zhai Qiong-Xiang 2 † Li Xiao-Jing 1 † Shi Zhen 1 Cheng Chuan-Fang 3 4 Fan Cui-Xia 3 4 Tang Bin 3 4 Zhang Ying 5 He Yun-Yan 3 4 Li Wen-Bin 3 4 Luo Sheng 3 4 Hou Chi 1 Chen Wen-Xiong 1 * Liao Wei-Ping 3 4 Wang Jie 3 4 * 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

Edited and reviewed by: Rossella Di Giaimo, University of Naples Federico II, Italy

 *Correspondence: Jie Wang wangjie2014010@163.com Wen-Xiong Chen chenwenxiong@gwcmc.org

†These authors have contributed equally to this work

 01 03 2024 2024 17 1385915 14 02 2024 19 02 2024 Copyright © 2024 Tian, Zhai, Li, Shi, Cheng, Fan, Tang, Zhang, He, Li, Luo, Hou, Chen, Liao and Wang. 2024 Tian, Zhai, Li, Shi, Cheng, Fan, Tang, Zhang, He, Li, Luo, Hou, Chen, Liao and Wang

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 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 ATP6V0C loss of function febrile seizures epilepsy with febrile seizures plus whole-exome sequencing section-at-acceptance Molecular Signalling and Pathways

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.

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.