Yang Tian
Yang Tian
1Department of Neurology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China
1,†,
Qiong-Xiang Zhai
Qiong-Xiang Zhai
2Department of Pediatrics, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China
2,†,
Xiao-Jing Li
Xiao-Jing Li
1Department of Neurology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China
1,†,
Zhen Shi
Zhen Shi
1Department of Neurology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China
1,
Chuan-Fang Cheng
Chuan-Fang Cheng
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
3,4,
Cui-Xia Fan
Cui-Xia Fan
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
3,4,
Bin Tang
Bin Tang
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
3,4,
Ying Zhang
Ying Zhang
5The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, China
5,
Yun-Yan He
Yun-Yan He
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
3,4,
Wen-Bin Li
Wen-Bin Li
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
3,4,
Sheng Luo
Sheng Luo
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
3,4,
Chi Hou
Chi Hou
1Department of Neurology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China
1,
Wen-Xiong Chen
Wen-Xiong Chen
1Department of Neurology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China
1,*,
Wei-Ping Liao
Wei-Ping Liao
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
3,4,
Jie Wang
Jie Wang
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
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
Received 2024 Feb 14; Accepted 2024 Feb 19; Collection date 2024.
Keywords: ATP6V0C, loss of function, febrile seizures, epilepsy with febrile seizures plus, whole-exome sequencing
Copyright © 2024 Tian, Zhai, Li, Shi, Cheng, Fan, Tang, Zhang, He, Li, Luo, Hou, Chen, Liao and Wang.
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