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Segregation of ATP10B variants in families with autosomal recessive parkinsonism.
Tesson, Christelle; Lohmann, Ebba; Devos, David; Bertrand, Hélène; Lesage, Suzanne; Brice, Alexis.
Afiliação
  • Tesson C; Sorbonne Université, Institut du Cerveau-Paris Brain Institute-ICM, Hôpital de la Salpêtrière, Inserm U 1127, CNRS UMR 7225, 75013, Paris, France.
  • Lohmann E; Department of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.
  • Devos D; Department of Medical Pharmacology, Department of Neurology, University Hospital, University of Lille, Neuroscience and Cognition, Inserm, UMR-S1172, Lille, France.
  • Bertrand H; Sorbonne Université, Institut du Cerveau-Paris Brain Institute-ICM, Hôpital de la Salpêtrière, Inserm U 1127, CNRS UMR 7225, 75013, Paris, France.
  • Lesage S; Sorbonne Université, Institut du Cerveau-Paris Brain Institute-ICM, Hôpital de la Salpêtrière, Inserm U 1127, CNRS UMR 7225, 75013, Paris, France.
  • Brice A; Sorbonne Université, Institut du Cerveau-Paris Brain Institute-ICM, Hôpital de la Salpêtrière, Inserm U 1127, CNRS UMR 7225, 75013, Paris, France. alexis.brice@icm-institute.org.
Acta Neuropathol ; 140(5): 783-785, 2020 11.
Article em En | MEDLINE | ID: mdl-32892229
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Transtornos Parkinsonianos Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
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PubMed Links
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Transtornos Parkinsonianos Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article