Segregation of ATP10B variants in families with autosomal recessive parkinsonism.

Autor: 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.; Département de Génétique, APHP, Hôpital de la Pitié Salpêtrière, 75013, Paris, France. alexis.brice@icm-institute.org.
Jazyk: angličtina
Zdroj: Acta neuropathologica [Acta Neuropathol] 2020 Nov; Vol. 140 (5), pp. 783-785. Date of Electronic Publication: 2020 Sep 05.
DOI: 10.1007/s00401-020-02219-6
Databáze: MEDLINE