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UNC13B variants associated with partial epilepsy with favourable outcome.
Wang, Jie; Qiao, Jing-Da; Liu, Xiao-Rong; Liu, De-Tian; Chen, Yan-Hui; Wu, Yi; Sun, Yan; Yu, Jing; Ren, Rong-Na; Mei, Zhen; Liu, Yu-Xi; Shi, Yi-Wu; Jiang, Mi; Lin, Si-Mei; He, Na; Li, Bin; Bian, Wen-Jun; Li, Bing-Mei; Yi, Yong-Hong; Su, Tao; Liu, Han-Kui; Gu, Wei-Yue; Liao, Wei-Ping.
  • Wang J; Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University, Guangzhou 510260, China.
  • Qiao JD; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou 510260, China.
  • Liu XR; Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University, Guangzhou 510260, China.
  • Liu DT; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou 510260, China.
  • Chen YH; Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University, Guangzhou 510260, China.
  • Wu Y; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou 510260, China.
  • Sun Y; Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University, Guangzhou 510260, China.
  • Yu J; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou 510260, China.
  • Ren RN; Department of Pediatrics, Fujian Medical University Union Hospital, Fujian 350001, China.
  • Mei Z; Department of Pediatrics, Fujian Medical University Union Hospital, Fujian 350001, China.
  • Liu YX; Department of Pediatrics, People's Hospital of Xinjiang Uygur Autonomous Region, Urumqi, Xinjiang 830001, China.
  • Shi YW; Department of Pediatrics, People's Hospital of Xinjiang Uygur Autonomous Region, Urumqi, Xinjiang 830001, China.
  • Jiang M; Department of Pediatrics and Neurosurgery, 900 Hospital of the Joint Logistics Team, Fujian 350025, China.
  • Lin SM; Department of Pediatrics and Neurosurgery, 900 Hospital of the Joint Logistics Team, Fujian 350025, China.
  • He N; Department of Neurology, The First Affiliated Hospital of Shanxi Medical University, Shanxi 030001, China.
  • Li B; Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University, Guangzhou 510260, China.
  • Bian WJ; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou 510260, China.
  • Li BM; Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University, Guangzhou 510260, China.
  • Yi YH; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou 510260, China.
  • Su T; Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University, Guangzhou 510260, China.
  • Liu HK; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou 510260, China.
  • Gu WY; Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University, Guangzhou 510260, China.
  • Liao WP; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou 510260, China.
Brain ; 144(10): 3050-3060, 2021 11 29.
Article en En | MEDLINE | ID: mdl-33876820
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Variación Genética / Epilepsias Parciales / Proteínas del Tejido Nervioso Tipo de estudio: Risk_factors_studies Límite: Adolescent / Adult / Animals / Child / Child, preschool / Female / Humans / Male Idioma: En Año: 2021 Tipo del documento: Article
Texto completo
Imprimir
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PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Variación Genética / Epilepsias Parciales / Proteínas del Tejido Nervioso Tipo de estudio: Risk_factors_studies Límite: Adolescent / Adult / Animals / Child / Child, preschool / Female / Humans / Male Idioma: En Año: 2021 Tipo del documento: Article