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Recessively-Inherited Adult-Onset Alexander Disease Caused by a Homozygous Mutation in the GFAP Gene.
Fu, Mu-Hui; Chang, Yung-Yee; Lin, Ni-Hsuan; Yang, Ai-Wen; Chang, Chiung-Chih; Liu, Jia-Shou; Peng, Cheng-Huei; Wu, Kay L H; Perng, Ming-Der; Lan, Min-Yu.
Afiliación
  • Fu MH; Department of Neurology, Chang Gung University College of Medicine, Kaohsiung, Taiwan.
  • Chang YY; Department of Neurology, Chang Gung University College of Medicine, Kaohsiung, Taiwan.
  • Lin NH; Center for Parkinson's Disease, Kaohsiung Chang Gung Memorial Hospital, and Chang Gung University College of Medicine, Kaohsiung, Taiwan.
  • Yang AW; Institute of Molecular Medicine, College of Life Sciences, National Tsing Hua University, Hsinchu, Taiwan.
  • Chang CC; Institute of Molecular Medicine, College of Life Sciences, National Tsing Hua University, Hsinchu, Taiwan.
  • Liu JS; Department of Medical Science, College of Life Sciences, National Tsing Hua University, Hsinchu, Taiwan.
  • Peng CH; Department of Neurology, Chang Gung University College of Medicine, Kaohsiung, Taiwan.
  • Wu KLH; Department of Neurology, Chang Gung University College of Medicine, Kaohsiung, Taiwan.
  • Perng MD; Department of Neurology, Chang Gung University College of Medicine, Kaohsiung, Taiwan.
  • Lan MY; Institute for Translational Research in Biomedicine, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, Taiwan.
Mov Disord ; 35(9): 1662-1667, 2020 09.
Article en En | MEDLINE | ID: mdl-32374915
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedad de Alexander Tipo de estudio: Prognostic_studies Límite: Adolescent / Adult / Humans / Male Idioma: En Revista: Mov Disord Asunto de la revista: NEUROLOGIA Año: 2020 Tipo del documento: Article País de afiliación: Taiwán
Texto completo
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PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedad de Alexander Tipo de estudio: Prognostic_studies Límite: Adolescent / Adult / Humans / Male Idioma: En Revista: Mov Disord Asunto de la revista: NEUROLOGIA Año: 2020 Tipo del documento: Article País de afiliación: Taiwán