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VPS13D-related disorders presenting as a pure and complicated form of hereditary spastic paraplegia.
Koh, Kishin; Ishiura, Hiroyuki; Shimazaki, Haruo; Tsutsumiuchi, Michiko; Ichinose, Yuta; Nan, Haitian; Hamada, Shun; Ohtsuka, Toshihisa; Tsuji, Shoji; Takiyama, Yoshihisa.
Afiliación
  • Koh K; Department of Neurology, Graduate School of Medical Sciences, University of Yamanashi, Yamanashi, Japan.
  • Ishiura H; Department of Neurology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Shimazaki H; Division of Neurology, Department of Internal Medicine, Jichi Medical University School of Medicine, Tochigi, Japan.
  • Tsutsumiuchi M; Department of Neurology, Jichi Medical University Saitama Medical Center, Omiya, Japan.
  • Ichinose Y; Department of Neurology, Toranomon Hospital, Tokyo, Japan.
  • Nan H; Department of Neurology, Graduate School of Medical Sciences, University of Yamanashi, Yamanashi, Japan.
  • Hamada S; Department of Neurology, Graduate School of Medical Sciences, University of Yamanashi, Yamanashi, Japan.
  • Ohtsuka T; Department of Biochemistry, Graduate School of Medical Sciences, University of Yamanashi, Yamanashi, Japan.
  • Tsuji S; Department of Biochemistry, Graduate School of Medical Sciences, University of Yamanashi, Yamanashi, Japan.
  • Takiyama Y; Department of Molecular Neurology, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.
Mol Genet Genomic Med ; 8(3): e1108, 2020 03.
Article en En | MEDLINE | ID: mdl-31876103
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Paraplejía / Fenotipo / Proteínas Tipo de estudio: Prognostic_studies Idioma: En Revista: Mol Genet Genomic Med Año: 2020 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Paraplejía / Fenotipo / Proteínas Tipo de estudio: Prognostic_studies Idioma: En Revista: Mol Genet Genomic Med Año: 2020 Tipo del documento: Article