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Loss-of-function variants in NEK1 are associated with an increased risk of sporadic ALS in the Japanese population.
Naruse, Hiroya; Ishiura, Hiroyuki; Mitsui, Jun; Takahashi, Yuji; Matsukawa, Takashi; Yoshimura, Jun; Doi, Koichiro; Morishita, Shinichi; Goto, Jun; Toda, Tatsushi; Tsuji, Shoji.
Afiliação
  • Naruse H; Department of Neurology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Ishiura H; Department of Neurology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Mitsui J; Department of Neurology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Takahashi Y; Department of Molecular Neurology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Matsukawa T; Department of Neurology, National Center Hospital, National Center of Neurology and Psychiatry, Tokyo, Japan.
  • Yoshimura J; Department of Neurology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Doi K; Department of Molecular Neurology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Morishita S; Department of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, The University of Tokyo, Tokyo, Japan.
  • Goto J; School of Bioscience and Biotechnology, Tokyo University of Technology, Tokyo, Japan.
  • Toda T; Department of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, The University of Tokyo, Tokyo, Japan.
  • Tsuji S; Department of Neurology, International University of Health and Welfare Mita Hospital, Tokyo, Japan.
J Hum Genet ; 66(3): 237-241, 2021 Mar.
Article em En | MEDLINE | ID: mdl-32920598
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Povo Asiático / Quinase 1 Relacionada a NIMA / Mutação com Perda de Função / Esclerose Lateral Amiotrófica Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Japão
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Povo Asiático / Quinase 1 Relacionada a NIMA / Mutação com Perda de Função / Esclerose Lateral Amiotrófica Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Japão