Your browser doesn't support javascript.
loading
PLA2G6-associated neurodegeneration presenting as a complicated form of hereditary spastic paraplegia.
Koh, Kishin; Ichinose, Yuta; Ishiura, Hiroyuki; Nan, Haitian; Mitsui, Jun; Takahashi, Junya; Sato, Wakiro; Itoh, Yoshiaki; Hoshino, Kyoko; Tsuji, Shoji; Takiyama, Yoshihisa.
Afiliação
  • Koh K; Department of Neurology, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, Yamanashi, Japan.
  • Ichinose Y; Department of Neurology, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, Yamanashi, Japan.
  • Ishiura H; Department of Neurology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Nan H; Department of Neurology, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, Yamanashi, Japan.
  • Mitsui J; Department of Molecular Neurology, The University of Tokyo, Tokyo, Japan.
  • Takahashi J; Department of Pediatrics, National Mie Hospital, Mie, Japan.
  • Sato W; Department of Immunology, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan.
  • Itoh Y; Department of Neurology, Osaka City University, Osaka, Japan.
  • Hoshino K; Department of Pediatrics, Minamiwakayama Medical Center, Wakayama, Japan.
  • Tsuji S; Department of Molecular Neurology, The University of Tokyo, Tokyo, Japan.
  • Takiyama Y; International University of Health and Welfare Graduate School, Chiba, Japan.
J Hum Genet ; 64(1): 55-59, 2019 Jan.
Article em En | MEDLINE | ID: mdl-30302010
Assuntos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Paraplegia Espástica Hereditária / Doenças Neurodegenerativas / Transtornos Parkinsonianos / Fosfolipases A2 do Grupo VI / Mutação Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Aged / Child / Female / Humans / Infant / Male Idioma: En Revista: J Hum Genet Ano de publicação: 2019 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Paraplegia Espástica Hereditária / Doenças Neurodegenerativas / Transtornos Parkinsonianos / Fosfolipases A2 do Grupo VI / Mutação Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Aged / Child / Female / Humans / Infant / Male Idioma: En Revista: J Hum Genet Ano de publicação: 2019 Tipo de documento: Article