Correction: Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment

Affiliations

• ¹ Sorbonne Université, Institut du Cerveau-Paris Brain Institute (ICM), AP-HP, INSERM, CNRS, University Hospital Pitié-Salpêtrière, Paris, France.
• ² EPHE, PSL Research University, Neurogenetics Group, Paris, France.
• ³ Genetic Department, University Hospital Pitié-Salpêtrière, AP-HP, Paris, France.
• ⁴ Expert center for Neurogenetic Diseases, Department of Neurology, CHU Gui de Chauliac, MMDN, Univ Montpellier, INSERM, EPHE, Montpellier, France.
• ⁵ Neurological Department University Hospital Strasbourg, Strasbourg, France.
• ⁶ University Bordeaux, Laboratoire MRGM, INSERM U1211, Centre de Référence Neurogénétique, Service de Génétique Médicale, CHU Bordeaux, Bordeaux, France.
• ⁷ University Hospital Essen, Department of Neurology, Essen, Germany.
• ⁸ Department of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.
• ⁹ Université de Franche-Comté, Centre de Génétique Humaine, Centre Hospitalier Régional Universitaire, Besançon, France.
• ¹⁰ Neurodegenerative Brain Diseases Group, VIB Center for Molecular Neurology, Laboratory of Neurogenetics, Institute Born-Bunge and Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium.
• ¹¹ Sorbonne Université, Institut du Cerveau-Paris Brain Institute (ICM), AP-HP, INSERM, CNRS, University Hospital Pitié-Salpêtrière, Paris, France. alexandra.durr@icm-institute.org.