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Investigating DYT1 in a Taiwanese dystonia cohort.
Wu, Meng-Chen; Chang, Yung-Yee; Chen, Ying-Fa; Lan, Min-Yu; Chen, Pei-Lung; Tai, Chun-Hwei; Lin, Chin-Hsien.
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  • Wu MC; Department of Geriatrics and Gerontology, National Taiwan University Hospital, Taipei, Taiwan; Department of Neurology, National Taiwan University Hospital, Taipei, Taiwan. Electronic address: rebeccawu1001@gmail.com.
  • Chang YY; Department of Neurology, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, Taiwan; Center for Parkinson's Disease, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, Taiwan. Electronic address: changyy7@gmail.com.
  • Chen YF; Department of Neurology, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, Taiwan; Center for Parkinson's Disease, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, Taiwan. Electronic address: alpha0716@gmail.com.
  • Lan MY; Department of Neurology, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, Taiwan; Center for Parkinson's Disease, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, Taiwan. Electronic address: myl@ksts.seed.net.tw.
  • Chen PL; Department of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan; Graduate Institute of Medical Genomics and Proteomics, National Taiwan University College of Medicine, Taipei, Taiwan. Electronic address: paylong@gmail.com.
  • Tai CH; Department of Neurology, National Taiwan University Hospital, Taipei, Taiwan. Electronic address: chtai66@gmail.com.
  • Lin CH; Department of Neurology, National Taiwan University Hospital, Taipei, Taiwan. Electronic address: chlin@ntu.edu.tw.
J Formos Med Assoc ; 121(1 Pt 2): 375-380, 2022 Jan.
Article en En | MEDLINE | ID: mdl-34092466
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trastornos Distónicos / Enfermedades Genéticas Ligadas al Cromosoma X Tipo de estudio: Prognostic_studies / Systematic_reviews Límite: Adult / Child / Humans / Male País/Región como asunto: Asia Idioma: En Revista: J Formos Med Assoc Asunto de la revista: MEDICINA Año: 2022 Tipo del documento: Article
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trastornos Distónicos / Enfermedades Genéticas Ligadas al Cromosoma X Tipo de estudio: Prognostic_studies / Systematic_reviews Límite: Adult / Child / Humans / Male País/Región como asunto: Asia Idioma: En Revista: J Formos Med Assoc Asunto de la revista: MEDICINA Año: 2022 Tipo del documento: Article