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The New p.F1700L LRRK2 Variant Causes Parkinson's Disease by Extensively Increasing Kinase Activity.
Borsche, Max; Pratuseviciute, Neringa; Schaake, Susen; Hinrichs, Frauke; Morel, Gabriel; Uter, Jan; Lohmann, Katja; Klein, Christine; Alessi, Dario R; Hagenah, Johann; Sammler, Esther.
Afiliação
  • Borsche M; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
  • Pratuseviciute N; Department of Neurology, University of Lübeck, Lübeck, Germany.
  • Schaake S; MRC Protein Phosphorylation and Ubiquitylation Unit, School of Life Sciences, University of Dundee, Dundee, United Kingdom.
  • Hinrichs F; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
  • Morel G; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
  • Uter J; MRC Protein Phosphorylation and Ubiquitylation Unit, School of Life Sciences, University of Dundee, Dundee, United Kingdom.
  • Lohmann K; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
  • Klein C; Department of Neurology, University of Lübeck, Lübeck, Germany.
  • Alessi DR; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
  • Hagenah J; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
  • Sammler E; MRC Protein Phosphorylation and Ubiquitylation Unit, School of Life Sciences, University of Dundee, Dundee, United Kingdom.
Mov Disord ; 38(6): 1105-1107, 2023 06.
Article em En | MEDLINE | ID: mdl-36971062
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson Tipo de estudo: Etiology_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
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PubMed Links
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson Tipo de estudo: Etiology_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article