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PRRT2 gene mutations associated with infantile convulsions induced by sucking and the genotype-phenotype correlation.
Liu, De-Tian; Tang, Xue-Qing; Wan, Rui-Ping; Luo, Sheng; Guan, Bao-Zhu; Li, Bin; Liu, Li-Hong; Li, Bing-Mei; Liu, Zhi-Gang; Xie, Long-Shan; Yi, Yong-Hong.
Afiliação
  • Liu DT; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
  • Tang XQ; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
  • Wan RP; Department of Pediatrics, Foshan Women and Children Hospital Affiliated to Southern Medical University, Foshan, China.
  • Luo S; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
  • Guan BZ; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
  • Li B; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
  • Liu LH; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
  • Li BM; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
  • Liu ZG; Department of Pediatrics, Foshan Women and Children Hospital Affiliated to Southern Medical University, Foshan, China.
  • Xie LS; First People's Hospital of Foshan, Foshan, China.
  • Yi YH; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Front Neurol ; 13: 836048, 2022.
Article em En | MEDLINE | ID: mdl-35959395
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Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: Front Neurol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: Front Neurol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China