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The ALOXE3 gene variants from patients with Dravet syndrome decrease gene expression and enzyme activity.
Gao, Mei-Mei; Huang, Hao-Ying; Chen, Si-Yu; Tang, Hui-Ling; He, Na; Feng, Wen-Cai; Lu, Ping; Hu, Fei; Yan, Hua-Juan; Long, Yue-Sheng.
Afiliação
  • Gao MM; Institute of Neuroscience and the Second Affiliated Hospital of Guangzhou Medical University, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, 250 Changang East Road, Guangzhou, 510260, China.
  • Huang HY; Institute of Neuroscience and the Second Affiliated Hospital of Guangzhou Medical University, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, 250 Changang East Road, Guangzhou, 510260, China.
  • Chen SY; Institute of Neuroscience and the Second Affiliated Hospital of Guangzhou Medical University, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, 250 Changang East Road, Guangzhou, 510260, China.
  • Tang HL; Institute of Neuroscience and the Second Affiliated Hospital of Guangzhou Medical University, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, 250 Changang East Road, Guangzhou, 510260, China.
  • He N; Department of Neurology, the Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, 510260, China.
  • Feng WC; Institute of Neuroscience and the Second Affiliated Hospital of Guangzhou Medical University, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, 250 Changang East Road, Guangzhou, 510260, China.
  • Lu P; Institute of Neuroscience and the Second Affiliated Hospital of Guangzhou Medical University, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, 250 Changang East Road, Guangzhou, 510260, China.
  • Hu F; Institute of Neuroscience and the Second Affiliated Hospital of Guangzhou Medical University, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, 250 Changang East Road, Guangzhou, 510260, China.
  • Yan HJ; Institute of Neuroscience and the Second Affiliated Hospital of Guangzhou Medical University, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, 250 Changang East Road, Guangzhou, 510260, China.
  • Long YS; Institute of Neuroscience and the Second Affiliated Hospital of Guangzhou Medical University, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, 250 Changang East Road, Guangzhou, 510260, China. Electronic address: longyuesheng@gzhmu.edu
Brain Res Bull ; 170: 81-89, 2021 05.
Article em En | MEDLINE | ID: mdl-33581311
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encéfalo / Epilepsias Mioclônicas / Lipoxigenase / Mutação Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
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PubMed Links
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encéfalo / Epilepsias Mioclônicas / Lipoxigenase / Mutação Idioma: En Ano de publicação: 2021 Tipo de documento: Article