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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.
Affiliation
  • 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 in En | MEDLINE | ID: mdl-36155026
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spastic Paraplegia, Hereditary Limits: Humans Language: En Journal: Parkinsonism Relat Disord Journal subject: NEUROLOGIA Year: 2022 Document type: Article Affiliation country:
Fulltext
Add to My VHL
Print
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PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spastic Paraplegia, Hereditary Limits: Humans Language: En Journal: Parkinsonism Relat Disord Journal subject: NEUROLOGIA Year: 2022 Document type: Article Affiliation country: