Editorial: Sub-molecular mechanism of genetic epilepsy by Wei-Ping Liao, Wei-Ping Liao, Qian Chen, Yu-Wu Jiang, Sheng Luo, Sheng Luo, Xiao-Rong Liu, Xiao-Rong Liu

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YWHAG Mutations Cause Childhood Myoclonic Epilepsy and Febrile Seizures: Molecular Sub-regional Effect and Mechanism by Xing-Guang Ye, Zhi-Gang Liu, Zhi-Gang Liu, Jie Wang, Jie Wang, Jie-Min Dai, Pei-Xiu Qiao, Ping-Ming Gao, Wei-Ping Liao, Wei-Ping Liao

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Critical Role of E1623 Residue in S3-S4 Loop of Nav1.1 Channel and Correlation Between Nature of Substitution and Functional Alteration by Tao Su, Tao Su, Meng-Long Chen, Meng-Long Chen, Li-Hong Liu, Li-Hong Liu, Hen Meng, Hen Meng, Bin Tang, Bin Tang, Xiao-Rong Liu, Xiao-Rong Liu, Wei-Ping Liao, Wei-Ping Liao

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Recessive PKD1 Mutations Are Associated With Febrile Seizures and Epilepsy With Antecedent Febrile Seizures and the Genotype-Phenotype Correlation by Jing-Yang Wang, Jing-Yang Wang, Jie Wang, Jie Wang, Xin-Guo Lu, Wang Song, Wang Song, Sheng Luo, Sheng Luo, Dong-Fang Zou, Li-Dong Hua, Qian Peng, Yang Tian, Liang-Di Gao, Liang-Di Gao, Wei-Ping Liao, Wei-Ping Liao, Na He, Na He

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Association of LONP1 gene with epilepsy and the sub-regional effect by Si-Xiu Li, Na He, Jian-Xiang Liao, Xin-Guo Lu, Wen-Guang Hu, Xiao-Rong Liu, Wei-Ping Liao, Xing-Wang Song, Bin Li

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ATP6V0C Is Associated With Febrile Seizures and Epilepsy With Febrile Seizures Plus by Yang Tian, Qiong-Xiang Zhai, Xiao-Jing Li, Zhen Shi, Chuan-Fang Cheng, Chuan-Fang Cheng, Cui-Xia Fan, Cui-Xia Fan, Bin Tang, Bin Tang, Ying Zhang, Yun-Yan He, Yun-Yan He, Wen-Bin Li, Wen-Bin Li, Sheng Luo, Sheng Luo, Chi Hou, Wen-Xiong Chen, Wei-Ping Liao, Wei-Ping Liao, Jie Wang, Jie Wang

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Corrigendum: ATP6V0C is associated with febrile seizures and epilepsy with febrile seizures plus by Yang Tian, Qiong-Xiang Zhai, Xiao-Jing Li, Zhen Shi, Chuan-Fang Cheng, Chuan-Fang Cheng, Cui-Xia Fan, Cui-Xia Fan, Bin Tang, Bin Tang, Ying Zhang, Yun-Yan He, Yun-Yan He, Wen-Bin Li, Wen-Bin Li, Sheng Luo, Sheng Luo, Chi Hou, Wen-Xiong Chen, Wei-Ping Liao, Wei-Ping Liao, Jie Wang, Jie Wang

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RYR2 Mutations Are Associated With Benign Epilepsy of Childhood With Centrotemporal Spikes With or Without Arrhythmia by Mei-Gang Ma, Mei-Gang Ma, Xiao-Rong Liu, Yuan Wu, Jie Wang, Bing-Mei Li, Yi-Wu Shi, Tao Su, Bin Li, De-Tian Liu, Yong-Hong Yi, Wei-Ping Liao

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Heterozygous PGM3 Variants Are Associated With Idiopathic Focal Epilepsy With Incomplete Penetrance by Xiao-Rong Liu, Wen-Jun Bian, Jie Wang, Ting-Ting Ye, Bing-Mei Li, De-Tian Liu, Bin Tang, Wei-Wen Deng, Yi-Wu Shi, Tao Su, Yong-Hong Yi, Wei-Ping Liao

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GRIN2A Variants Associated With Idiopathic Generalized Epilepsies by Xiao-Rong Liu, Xing-Xing Xu, Si-Mei Lin, Cui-Ying Fan, Ting-Ting Ye, Bin Tang, Yi-Wu Shi, Tao Su, Bing-Mei Li, Yong-Hong Yi, Jian-Hong Luo, Wei-Ping Liao

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HLA-B*13:01 as a Risk Allele for Antiepileptic Drugs-Induced Cutaneous Adverse Reactions: Higher Risk for Cross-Reactivity? by Fu-Li Min, Fu-Li Min, Bi-Jun Mao, Zhong-Zheng Zheng, Na He, Cui-Xia Fan, Rui-Yan Cai, Juan Wang, Yang-Mei Ou, Bing Qin, Wei-Ping Liao, Yong-Hong Yi, Ze Li, Yi-Wu Shi

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DLG3 variants caused X-linked epilepsy with/without neurodevelopmental disorders and the genotype-phenotype correlation by Yun-Yan He, Yun-Yan He, Sheng Luo, Liang Jin, Liang Jin, Peng-Yu Wang, Jie Xu, Hong-Liang Jiao, Hong-Jun Yan, Yao Wang, Qiong-Xiang Zhai, Jing-Jing Ji, Weng-Jun Zhang, Peng Zhou, Hua Li, Wei-Ping Liao, Song Lan, Lin Xu

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DEPDC5 Variants Associated Malformations of Cortical Development and Focal Epilepsy With Febrile Seizure Plus/Febrile Seizures: The Role of Molecular Sub-Regional Effect by Liu Liu, Liu Liu, Zi-Rong Chen, Zi-Rong Chen, Hai-Qing Xu, De-Tian Liu, Yong Mao, Han-Kui Liu, Xiao-Rong Liu, Peng Zhou, Si-Mei Lin, Bin Li, Na He, Tao Su, Qiong-Xiang Zhai, Heng Meng, Wei-Ping Liao, Yong-Hong Yi

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Recessive LAMA5 Variants Associated With Partial Epilepsy and Spasms in Infancy by Sheng Luo, Zhi-Gang Liu, Zhi-Gang Liu, Juan Wang, Jun-Xia Luo, Xing-Guang Ye, Xing-Guang Ye, Xin Li, Qiong-Xiang Zhai, Xiao-Rong Liu, Jie Wang, Liang-Di Gao, Fu-Li Liu, Zi-Long Ye, Huan Li, Zai-Fen Gao, Qing-Hui Guo, Bing-Mei Li, Yong-Hong Yi, Wei-Ping Liao

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HCFC1 variants in the proteolysis domain are associated with X‐linked idiopathic partial epilepsy: Exploring the underlying mechanism by Na He, Bao‐Zhu Guan, Jie Wang, Han‐Kui Liu, Yong Mao, Zhi‐Gang Liu, Fei Yin, Jing Peng, Bo Xiao, Bei‐sha Tang, Dong Zhou, Guang Huang, Qi‐Lin Dai, Ying Zeng, Hong Han, Qiong‐Xiang Zhai, Bin Li, Bin Tang, Wen‐Bin Li, Wang Song, Liu Liu, Yi‐Wu Shi, Bing‐Mei Li, Tao Su, Peng Zhou, Xiao‐Rong Liu, Li‐Wu Guo, Yong‐Hong Yi, Wei‐Ping Liao

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