Abstract
A Correction to this paper has been published: https://doi.org/10.1038/s41436-020-01064-y
- Title
- Correction: Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment
- Creators - without role
- Thomas Roux - Institut du CerveauMathieu Barbier - Institut du CerveauMélanie Papin - Institut du CerveauClaire-Sophie Davoine - Institut du CerveauSabrina Sayah - Institut du CerveauGiulia Coarelli - Institut du CerveauPerrine Charles - Pitié-Salpêtrière HospitalCecilia Marelli - InsermLivia Parodi - Institut du CerveauChristine Tranchant - University of StrasbourgCyril Goizet - InsermStephan Klebe - Essen University HospitalEbba Lohmann - Hertie Institute for Clinical Brain ResearchLionel Van Maldergem - Université de Franche-Comté, Centre de Génétique Humaine, Centre Hospitalier Régional Universitaire, Besançon, France.Christine van Broeckhoven - VIB-UAntwerp Center for Molecular NeurologyMarie Coutelier - Institut du CerveauChristelle Tesson - InsermGiovanni Stevanin - Institut du CerveauCharles Duyckaerts - Institut du CerveauAlexis Brice - InsermAlexandra Durr - InsermAlexandra Durr - InsermGiovanni Stevanin - Institut du CerveauAlexis Brice - InsermFrédéric Darios - Pitié-Salpêtrière HospitalSylvie Forlani - Pitié-Salpêtrière HospitalPitié-Salpêtrière Site - UF de Neurogénétique Moléculaire et Cellulaire, Paris, FranceGuillaume Banneau - UF de Neurogénétique Moléculaire et Cellulaire, Paris, FranceCécile Cazeneuve - UF de Neurogénétique Moléculaire et Cellulaire, Paris, FrancePerrine Charles - Pitié-Salpêtrière HospitalCharles Duyckaerts - Institut du CerveauBertrand Fontaine - Service de Neurologie et Pathologies du Mouvement Hôpital d’Adultes de la Timone, Marseille, FranceJean-Philippe Azulay - Service de Neurologie et Pathologies du Mouvement Hôpital d’Adultes de la Timone, Marseille, FranceOdile Boesfplug-Tanguy - Hôpital Robert-DebréCyril Goizet - InsermDidier Hannequin - Unité de Génétique Clinique Hôpital Charles Nicolle, Rouen, FranceJamilé Hazan - Marie CurieAndrea Burgo - EvryChristophe Verny - Service de Génétique Département de Neurologie, Unité Charcot, CHU d’Angers, Angers, FranceMichel Koenig - Institut Universitaire de Recherche CliniquePierre Labauge - Service de Neurologie Hôpital Caremeau, Place du Professeur Debré, Nîmes, FranceCecilia Marelli - InsermKarine N’guyen - Hôpital d'EnfantsDiana Rodriguez - Hôpital Armand-TrousseauSoraya Belarbi - Marine AcousticsAbdelmadjid Hamri - Service de Neurologie Hôpital Benbadis, Constantine, AlgeriaMeriem Tazir - Marine AcousticsSylvia Boesch - Neurology, Medical University, Innsbruck, AustriaMassimo Pandolfo - Université Libre de BruxellesJardim Laura - Universidade Federal do Rio Grande do SulVelina Guergueltcheva - Clinic of Neurology, University Hospital Alexandrovska, Sofia, BulgariaIvalo Tournev - Clinic of Neurology, University Hospital Alexandrovska, Sofia, BulgariaOlga Lucia Pedraza Linarès - Departamento Neurociencias Faculté de Médecine, Cra. 18 No. 88-17 (Cons. 305), FUCS, HIUSJ, Bogota, ColombiaJørgen E. Nielsen - University of CopenhagenKirsten Svenstrup - University of CopenhagenMaha Zaki - Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, EgyptPeter Bauer - University of TübingenLüdger Schöls - University of TübingenRebecca Schüle - University of TübingenAlexander Lossos - Department of Neurology Hadassah-Hebrew University Hospital, Ein Kerem, Jerusalem, IsraelMaria-Teresa Bassi - Eugenio Medea, Bosisio Parini, ItalyManuela Basso - University of TrentoEnrico Bertini - Molecular Medicine & Department of Neurosciences Osp. Bambino Gesù, Roma, ItalyAlfredo Brusco - University of TurinCarlo Casali - Sapienza University of RomeGiorgio Casari - Vita-Salute San Raffaele UniversityChiara Criscuolo - StudiAlessandro Filla - StudiLaura Orsi - Department of Neuroscience and Mental Health–Neurological Clinic 1, Universitary Hospital Torino, Turin, ItalyFilippo M. Santorelli - Fondazione Stella MarisEnza Maria Valente - CSSMarinela Vavla - IRCCS Eugenio MedeaGiovanni Vazza - StudiAndré Megarbane - Unité de génétique Médicale Université Saint-Joseph Faculté de Médecine, Campus des Sciences Médicales, Rue de Damas, Beirut, LebanonAli Benomar - Service de Neurologie B Laboratoire de Neurogénétique, Hôpital des Spécialités, Rabat Instituts, Rabat, MoroccoBerry Kremer - Radboud University Medical CenterWilleke Van Roon-Mom - Leiden University Medical CenterRichard Roxburgh - Auckland City HospitalAnne Kjersti Erichsen - Department of Neurology Ullevål University Hospital, Oslo, NorwayChantal Tallaksen - Department of Neurology Ullevål University Hospital, Oslo, NorwayIsabel Alonso - Universidade do PortoPaula Coutinho - Serviço de Neurologia Hospital S. Sebastião, Santa Maria da Feira, PortugalJosé Léal Loureiro - Serviço de Neurologia Hospital S. Sebastião, Santa Maria da Feira, PortugalJorge Sequeiros - Universidade do PortoMustapha Salih - King Khalid University HospitalVladimir S Kostic - Institute of Neurology Clinical Centre of Serbia, Belgrade, SerbiaIdoia Rouco Axpe - BioCruces Health Research Center Institute, Barakaldo, SpainLiena Elsayed - University of KhartoumMartin Arce Paucar - Department of Clinical Neuroscience, Karolinska University, Stockholm, SwedenSamir Roumani - Service of Neurology, Damascus, SyriaSoong Bing-Wen - National Yang Ming UniversityEvan Reid - University of CambridgeNethisinghe Suran - UCL Institute of Neurology London, London, United KingdomThomas Warner - University Department of Clinical Neurosciences Royal Free and University College Medical School, University College, London, United KingdomNicholas Wood - National Hospital for Neurology and NeurosurgerySPATAX network
- Publication Details
- Genetics in medicine, Vol.23(10), pp.2021-2021
- Publisher
- Elsevier Inc
- Identifiers
- 9927963408331
- Academic Unit
- Princess Nourah bint Abdulrahman University
- Language
- English
- Resource Type
- Journal article