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A new F-box protein 7 gene mutation causing typical Parkinson's disease.
Lohmann, Ebba; Coquel, Anne-Sophie; Honoré, Aurélie; Gurvit, Hakan; Hanagasi, Hasmet; Emre, Murat; Leutenegger, Anne L; Drouet, Valérie; Sahbatou, Mourad; Guven, Gamze; Erginel-Unaltuna, Nihan; Deleuze, Jean-Francois; Lesage, Suzanne; Brice, Alexis.
Afiliação
  • Lohmann E; Behavioral Neurology and Movement Disorders Unit, Department of Neurology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.
  • Coquel AS; Department of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tübingen, and DZNE, German Center for Neurodegenerative Diseases, Tübingen, Germany.
  • Honoré A; Sorbonne Université, UPMC Univ Paris 06, UM 1127, ICM, Paris, France; Inserm, U 1127, ICM, Paris, France; Cnrs, UMR 7225, ICM, Paris, France; ICM, Paris, F-75013, Paris, France.
  • Gurvit H; Sorbonne Université, UPMC Univ Paris 06, UM 1127, ICM, Paris, France; Inserm, U 1127, ICM, Paris, France; Cnrs, UMR 7225, ICM, Paris, France; ICM, Paris, F-75013, Paris, France.
  • Hanagasi H; Behavioral Neurology and Movement Disorders Unit, Department of Neurology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.
  • Emre M; Behavioral Neurology and Movement Disorders Unit, Department of Neurology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.
  • Leutenegger AL; Behavioral Neurology and Movement Disorders Unit, Department of Neurology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.
  • Drouet V; Inserm, U946, Paris, France; Université Paris Diderot, Institut Universitaire d'Hématologie, Paris, France.
  • Sahbatou M; Sorbonne Université, UPMC Univ Paris 06, UM 1127, ICM, Paris, France; Inserm, U 1127, ICM, Paris, France; Cnrs, UMR 7225, ICM, Paris, France; ICM, Paris, F-75013, Paris, France.
  • Guven G; Fondation Jean Dausset, Centre d'Etude du Polymorphisme Humain (CEPH), Paris, France.
  • Erginel-Unaltuna N; Institute for Experimental Medicine, Genetics Department, Istanbul University, Istanbul, Turkey.
  • Deleuze JF; Institute for Experimental Medicine, Genetics Department, Istanbul University, Istanbul, Turkey.
  • Lesage S; Commissariat à l'Energie Atomique, Institut de Génomique, Centre National de Génotypage, Evry, France.
  • Brice A; Sorbonne Université, UPMC Univ Paris 06, UM 1127, ICM, Paris, France; Inserm, U 1127, ICM, Paris, France; Cnrs, UMR 7225, ICM, Paris, France; ICM, Paris, F-75013, Paris, France.
Mov Disord ; 30(8): 1130-3, 2015 Jul.
Article em En | MEDLINE | ID: mdl-26010069
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Proteínas F-Box Tipo de estudo: Prognostic_studies Limite: Aged80 / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Revista: Mov Disord Ano de publicação: 2015 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: Doença de Parkinson / Proteínas F-Box Tipo de estudo: Prognostic_studies Limite: Aged80 / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Revista: Mov Disord Ano de publicação: 2015 Tipo de documento: Article