Your browser doesn't support javascript.
loading
Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene.
Yin, Xiao-Meng; Lin, Jing-Han; Cao, Li; Zhang, Tong-Mei; Zeng, Sheng; Zhang, Kai-Lin; Tian, Wo-Tu; Hu, Zheng-Mao; Li, Nan; Wang, Jun-Ling; Guo, Ji-Feng; Wang, Ruo-Xi; Xia, Kun; Zhang, Zhuo-Hua; Yin, Fei; Peng, Jing; Liao, Wei-Ping; Yi, Yong-Hong; Liu, Jing-Yu; Yang, Zhi-Xian; Chen, Zhong; Mao, Xiao; Yan, Xin-Xiang; Jiang, Hong; Shen, Lu; Chen, Sheng-Di; Zhang, Li-Ming; Tang, Bei-Sha.
Afiliação
  • Yin XM; Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
  • Lin JH; Department of Neurology, The First Affiliated Hospital of Harbin Medical University, Harbin 150001, China.
  • Cao L; Department of Neurology and Institute of Neurology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
  • Zhang TM; Department of Physiology, School of Basic Medicine and Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
  • Zeng S; The Institute for Brain Research, Collaborative Innovation Center for Brain Science, Huazhong University of Science and Technology, Wuhan 430030, China.
  • Zhang KL; Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
  • Tian WT; Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
  • Hu ZM; Department of Neurology and Institute of Neurology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
  • Li N; Center for Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan 410008, China.
  • Wang JL; Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
  • Guo JF; Key Laboratory of Hunan Province in Neurodegenerative Disorders, Central South University, Changsha, Hunan 410008, China.
  • Wang RX; Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
  • Xia K; Center for Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan 410008, China.
  • Zhang ZH; Key Laboratory of Hunan Province in Neurodegenerative Disorders, Central South University, Changsha, Hunan 410008, China.
  • Yin F; Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
  • Peng J; Center for Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan 410008, China.
  • Liao WP; National Clinical Research Center for Geriatric Disorders, Central South University, Changsha, Hunan 410008, China.
  • Yi YH; Key Laboratory of Hunan Province in Neurodegenerative Disorders, Central South University, Changsha, Hunan 410008, China.
  • Liu JY; Center for Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan 410008, China.
  • Yang ZX; Institute of Precision Medicine, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
  • Chen Z; Center for Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan 410008, China.
  • Mao X; Center for Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan 410008, China.
  • Yan XX; Institute of Precision Medicine, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
  • Jiang H; Department of Neurosciences, School of Medicine, University of South China, Hengyang, Hunan 420001, China.
  • Shen L; Department of Pediatrics, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
  • Chen SD; Hunan Intellectual and Development Disabilities Research Center, Changsha, Hunan 410008, China.
  • Zhang LM; Department of Pediatrics, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
  • Tang BS; Hunan Intellectual and Development Disabilities Research Center, Changsha, Hunan 410008, China.
Hum Mol Genet ; 27(4): 757-758, 2018 02 15.
Article em En | MEDLINE | ID: mdl-29351621
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: China
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: China