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DLG3 variants caused X-linked epilepsy with/without neurodevelopmental disorders and the genotype-phenotype correlation.
He, Yun-Yan; Luo, Sheng; Jin, Liang; Wang, Peng-Yu; Xu, Jie; Jiao, Hong-Liang; Yan, Hong-Jun; Wang, Yao; Zhai, Qiong-Xiang; Ji, Jing-Jing; Zhang, Weng-Jun; Zhou, Peng; Li, Hua; Liao, Wei-Ping; Lan, Song; Xu, Lin.
Afiliação
  • He YY; Department of Neurology, Women and Children's Hospital, Qingdao University, Qingdao, China.
  • Luo S; 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.
  • Jin 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.
  • Wang PY; 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.
  • Xu J; Department of Neurology, The Affiliated Nanhua Hospital, Hengyang Medical School, University of South China, Hengyang, China.
  • Jiao HL; 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.
  • Yan HJ; 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 Y; Department of Neurosurgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
  • Zhai QX; Epilepsy Center, Guangdong 999 Brain Hospital, Guangzhou, China.
  • Ji JJ; Epilepsy Center, Guangdong 999 Brain Hospital, Guangzhou, China.
  • Zhang WJ; Department of Pediatrics, Guangdong General Hospital, Guangdong Academy of Medical Sciences, 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.
  • Li H; 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.
  • Lan S; Epilepsy Center, Guangdong 999 Brain Hospital, Guangzhou, China.
  • Xu 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.
Front Mol Neurosci ; 16: 1290919, 2023.
Article em En | MEDLINE | ID: mdl-38249294

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Mol Neurosci Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Mol Neurosci Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China
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