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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.
Affiliation
  • 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 de En | MEDLINE | ID: mdl-35959395
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Type d'étude: Risk_factors_studies Langue: En Journal: Front Neurol Année: 2022 Type de document: Article Pays d'affiliation: Chine Pays de publication: Suisse
Texte intégral
Ajouter à My VHL
Imprimer
XML
PubMed Links
Recherche sur Google

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Type d'étude: Risk_factors_studies Langue: En Journal: Front Neurol Année: 2022 Type de document: Article Pays d'affiliation: Chine Pays de publication: Suisse