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Stop-gain mutations in UBAP1 cause pure autosomal-dominant spastic paraplegia.
Lin, Xiang; Su, Hui-Zhen; Dong, En-Lin; Lin, Xiao-Hong; Zhao, Miao; Yang, Can; Wang, Chong; Wang, Jie; Chen, Yi-Jun; Yu, Hongjie; Xu, Jianfeng; Ma, Li-Xiang; Xiong, Zhi-Qi; Wang, Ning; Chen, Wan-Jin.
Affiliation
  • Lin X; Department of Neurology and Institute of Neurology, The First Affiliated Hospital of Fujian Medical University, Fuzhou 350005, China.
  • Su HZ; Fujian Key Laboratory of Molecular Neurology, Fujian Medical University, Fuzhou 350005, China.
  • Dong EL; Department of Neurology and Institute of Neurology, The First Affiliated Hospital of Fujian Medical University, Fuzhou 350005, China.
  • Lin XH; Department of Neurology and Institute of Neurology, The First Affiliated Hospital of Fujian Medical University, Fuzhou 350005, China.
  • Zhao M; Department of Neurology and Institute of Neurology, The First Affiliated Hospital of Fujian Medical University, Fuzhou 350005, China.
  • Yang C; Department of Neurology and Institute of Neurology, The First Affiliated Hospital of Fujian Medical University, Fuzhou 350005, China.
  • Wang C; Institute of Neuroscience and State Key Laboratory of Neuroscience, CAS Center for Excellence in Brain Science and Intelligence Technology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China.
  • Wang J; Department of Neurology and Institute of Neurology, The First Affiliated Hospital of Fujian Medical University, Fuzhou 350005, China.
  • Chen YJ; Institute of Neuroscience and State Key Laboratory of Neuroscience, CAS Center for Excellence in Brain Science and Intelligence Technology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China.
  • Yu H; Department of Neurology and Institute of Neurology, The First Affiliated Hospital of Fujian Medical University, Fuzhou 350005, China.
  • Xu J; Program for Personalized Cancer Care, NorthShore University HealthSystem, Evanston, IL 60201, USA.
  • Ma LX; Program for Personalized Cancer Care, NorthShore University HealthSystem, Evanston, IL 60201, USA.
  • Xiong ZQ; Department of Anatomy, Histology and Embryology, Shanghai Medical College, Fudan University, Shanghai 200032, China.
  • Wang N; Institute of Neuroscience and State Key Laboratory of Neuroscience, CAS Center for Excellence in Brain Science and Intelligence Technology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China.
  • Chen WJ; Department of Neurology and Institute of Neurology, The First Affiliated Hospital of Fujian Medical University, Fuzhou 350005, China.
Brain ; 142(8): 2238-2252, 2019 08 01.
Article in En | MEDLINE | ID: mdl-31203368
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spastic Paraplegia, Hereditary / Carrier Proteins Limits: Adolescent / Adult / Animals / Child / Female / Humans / Male / Middle aged Language: En Journal: Brain Year: 2019 Document type: Article Affiliation country: China Country of publication: Reino Unido
Fulltext
Add to My VHL
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spastic Paraplegia, Hereditary / Carrier Proteins Limits: Adolescent / Adult / Animals / Child / Female / Humans / Male / Middle aged Language: En Journal: Brain Year: 2019 Document type: Article Affiliation country: China Country of publication: Reino Unido