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Investigating KIF1A mutations in a Taiwanese cohort with hereditary spastic paraplegia.
Hsu, Shao-Lun; Liao, Yi-Chu; Lin, Kon-Ping; Lin, Po-Yu; Yu, Kai-Wei; Tsai, Yu-Shuen; Guo, Yuh-Cherng; Lee, Yi-Chung.
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  • Hsu SL; Department of Neurology, Taipei Veterans General Hospital, Taipei, Taiwan; Department of Neurology, National Yang Ming Chiao Tung University School of Medicine, Taipei, Taiwan.
  • Liao YC; Department of Neurology, Taipei Veterans General Hospital, Taipei, Taiwan; Department of Neurology, National Yang Ming Chiao Tung University School of Medicine, Taipei, Taiwan; Brain Research Center, National Yang Ming Chiao Tung University, Taipei, Taiwan.
  • Lin KP; Department of Neurology, Taipei Veterans General Hospital, Taipei, Taiwan; Department of Neurology, National Yang Ming Chiao Tung University School of Medicine, Taipei, Taiwan.
  • Lin PY; Department of Neurology, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
  • Yu KW; Department of Radiology, Taipei Veterans General Hospital, Taipei, Taiwan.
  • Tsai YS; Center for Systems and Synthetic Biology, National Yang Ming Chiao Tung University, Taipei, Taiwan.
  • Guo YC; Department of Neurology, China Medical University Hospital, Taichung, Taiwan; School of Medicine, China Medical University, Taichung, Taiwan; Neuroscience and Brain Disease Center, College of Medicine, China Medical University, Taichung, Taiwan. Electronic address: d24943@mail.cmuh.org.tw.
  • Lee YC; Department of Neurology, Taipei Veterans General Hospital, Taipei, Taiwan; Department of Neurology, National Yang Ming Chiao Tung University School of Medicine, Taipei, Taiwan; Brain Research Center, National Yang Ming Chiao Tung University, Taipei, Taiwan. Electronic address: ycli@vghtpe.gov.tw.
Parkinsonism Relat Disord ; 103: 144-149, 2022 10.
Article en En | MEDLINE | ID: mdl-36155026
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Paraplejía Espástica Hereditaria Límite: Humans Idioma: En Revista: Parkinsonism Relat Disord Asunto de la revista: NEUROLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Taiwán
Texto completo
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PubMed Links
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Paraplejía Espástica Hereditaria Límite: Humans Idioma: En Revista: Parkinsonism Relat Disord Asunto de la revista: NEUROLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Taiwán