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Hartnup disease presenting as hereditary spastic paraplegia and severe peripheral neuropathy.
Wang, Xianling; Li, Xu-Ying; Piao, Yueshan; Yuan, Guobin; Lin, Yicong; Chen, Hai; Wang, Zhanjun; Li, Cunjiang; Wang, Chaodong.
Afiliación
  • Wang X; Department of Neurology, Xuanwu Hospital of Capital Medical University, National Clinical Research Center for Geriatric Diseases, Beijing, China.
  • Li XY; Department of Neurology, Xuanwu Hospital of Capital Medical University, National Clinical Research Center for Geriatric Diseases, Beijing, China.
  • Piao Y; Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China.
  • Yuan G; Department of Neurology, Xuanwu Hospital of Capital Medical University, National Clinical Research Center for Geriatric Diseases, Beijing, China.
  • Lin Y; Department of Pathology, Xuanwu Hospital of Capital Medical University, Beijing, China.
  • Chen H; Department of Neurology, Xuanwu Hospital of Capital Medical University, National Clinical Research Center for Geriatric Diseases, Beijing, China.
  • Wang Z; Department of Neurology, Xuanwu Hospital of Capital Medical University, National Clinical Research Center for Geriatric Diseases, Beijing, China.
  • Li C; Department of Neurology, Xuanwu Hospital of Capital Medical University, National Clinical Research Center for Geriatric Diseases, Beijing, China.
  • Wang C; Department of Neurology, Xuanwu Hospital of Capital Medical University, National Clinical Research Center for Geriatric Diseases, Beijing, China.
Am J Med Genet A ; 188(1): 237-242, 2022 01.
Article en En | MEDLINE | ID: mdl-34459558
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Paraplejía Espástica Hereditaria / Enfermedad de Hartnup Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: China
Texto completo
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XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Paraplejía Espástica Hereditaria / Enfermedad de Hartnup Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: China