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HCFC1 variants in the proteolysis domain are associated with X-linked idiopathic partial epilepsy: Exploring the underlying mechanism.
He, Na; Guan, Bao-Zhu; Wang, Jie; Liu, Han-Kui; Mao, Yong; Liu, Zhi-Gang; Yin, Fei; Peng, Jing; Xiao, Bo; Tang, Bei-Sha; Zhou, Dong; Huang, Guang; Dai, Qi-Lin; Zeng, Ying; Han, Hong; Zhai, Qiong-Xiang; Li, Bin; Tang, Bin; Li, Wen-Bin; Song, Wang; Liu, Liu; Shi, Yi-Wu; Li, Bing-Mei; Su, Tao; Zhou, Peng; Liu, Xiao-Rong; Guo, Li-Wu; Yi, Yong-Hong; Liao, Wei-Ping.
Afiliação
  • He N; Department of Neurology, Institute of Neuroscience, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.
  • Guan BZ; Department of Neurology, Institute of Neuroscience, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.
  • Wang J; Department of Neurology, Institute of Neuroscience, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.
  • Liu HK; BGI-Genomics, BGI-Shenzhen, Shenzhen, China.
  • Mao Y; Frasergen Bioinformatics Co., Ltd, Wuhan, China.
  • Liu ZG; Department of Pediatrics, Affiliated Foshan Maternity and Child Healthcare Hospital, Southern Medical University, Foshan, China.
  • Yin F; Department of Pediatrics, Xiangya Hospital, Central South University, Changsha, China.
  • Peng J; Department of Pediatrics, Xiangya Hospital, Central South University, Changsha, China.
  • Xiao B; Department of Neurology, Xiangya Hospital, Central South University, Changsha, China.
  • Tang BS; Department of Neurology, Xiangya Hospital, Central South University, Changsha, China.
  • Zhou D; Department of Neurology, West China Hospital, Sichuan University, Chengdu, China.
  • Huang G; Department of Pediatrics, The First Affiliated Hospital of Shantou University Medical College, Shantou, China.
  • Dai QL; Department of Neurology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
  • Zeng Y; Department of Neurology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
  • Han H; Department of Pediatrics, Children's Hospital of Shanxi, Taiyuan, China.
  • Zhai QX; Department of Pediatrics, Guangdong General Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.
  • Li B; Department of Neurology, Institute of Neuroscience, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.
  • Tang B; Department of Neurology, Institute of Neuroscience, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.
  • Li WB; Department of Neurology, Institute of Neuroscience, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.
  • Song W; Department of Neurology, Institute of Neuroscience, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.
  • Liu L; Department of Neurology, Institute of Neuroscience, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.
  • Shi YW; Department of Neurology, Institute of Neuroscience, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.
  • Li BM; Department of Neurology, Institute of Neuroscience, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.
  • Su T; Department of Neurology, Institute of Neuroscience, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.
  • Zhou P; Department of Neurology, Institute of Neuroscience, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.
  • Liu XR; Department of Neurology, Institute of Neuroscience, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.
  • Guo LW; Division of molecular testing, Bio Diagnostic laboratories, Brooklyn, New York, USA.
  • Yi YH; Department of Neurology, Institute of Neuroscience, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.
  • Liao WP; Department of Neurology, Institute of Neuroscience, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.
Clin Transl Med ; 13(6): e1289, 2023 06.
Article em En | MEDLINE | ID: mdl-37264743
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Epilepsias Parciais / Epilepsia Tipo de estudo: Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Humans Idioma: En Revista: Clin Transl Med Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Epilepsias Parciais / Epilepsia Tipo de estudo: Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Humans Idioma: En Revista: Clin Transl Med Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China