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Investigating ZFYVE26 mutations in a Taiwanese cohort with hereditary spastic paraplegia.
Hsu, Shao-Lun; Lu, Yi-Jiun; Tsai, Yu-Shuen; Chao, Hua-Chuan; Fuh, Jong-Ling; Liao, Yi-Chu; Lee, Yi-Chung.
Affiliation
  • Hsu SL; Department of Neurology, Neurological Institute, Taipei Veterans General Hospital, Taipei, Taiwan; Department of Neurology, National Yang-Ming University School of Medicine, Taipei, Taiwan.
  • Lu YJ; Department of Neurosurgery, Neurological Institute, Taipei Veterans General Hospital, Taipei, Taiwan.
  • Tsai YS; Center for Systems and Synthetic Biology, National Yang-Ming University, Taipei, Taiwan.
  • Chao HC; Division of Neurology, Department of Medicine, Taipei Veterans General Hospital, Taoyuan Branch, Taoyuan, Taiwan; Department of Neurology, National Yang-Ming University School of Medicine, Taipei, Taiwan.
  • Fuh JL; Department of Neurology, Neurological Institute, Taipei Veterans General Hospital, Taipei, Taiwan; Department of Neurology, National Yang-Ming University School of Medicine, Taipei, Taiwan; Brain Research Center, National Yang-Ming University School of Medicine, Taipei, Taiwan.
  • Liao YC; Department of Neurology, Neurological Institute, Taipei Veterans General Hospital, Taipei, Taiwan; Department of Neurology, National Yang-Ming University School of Medicine, Taipei, Taiwan; Brain Research Center, National Yang-Ming University School of Medicine, Taipei, Taiwan.
  • Lee YC; Department of Neurology, Neurological Institute, Taipei Veterans General Hospital, Taipei, Taiwan; Department of Neurology, National Yang-Ming University School of Medicine, Taipei, Taiwan; Brain Research Center, National Yang-Ming University School of Medicine, Taipei, Taiwan. Electronic address: y
J Formos Med Assoc ; 121(1 Pt 1): 126-133, 2022 Jan.
Article in En | MEDLINE | ID: mdl-33637369
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spastic Paraplegia, Hereditary / Carrier Proteins Type of study: Guideline / Prognostic_studies Limits: Humans Country/Region as subject: Asia Language: En Journal: J Formos Med Assoc Journal subject: MEDICINA Year: 2022 Document type: Article Affiliation country: Taiwan Country of publication: Singapore
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spastic Paraplegia, Hereditary / Carrier Proteins Type of study: Guideline / Prognostic_studies Limits: Humans Country/Region as subject: Asia Language: En Journal: J Formos Med Assoc Journal subject: MEDICINA Year: 2022 Document type: Article Affiliation country: Taiwan Country of publication: Singapore