Interrupted CAG expansions in ATXN2 gene expand the genetic spectrum of frontotemporal dementias
Year: 2018
Type: article
Abstract: Clemence Fournier and Vincent Anquetil contributed equally to this work.
Electronic supplementary material
The online version of this article (10.1186/s40478-018-0547-8) contains supplementary material, which is available to authorized users.
Authors: Neuro-CEB Neuropathology Network, Clémence Fournier, Vincent Anquetil, Agnès Camuzat, Sandrine Stirati-Buron, Véronique Sazdovitch, Laura Molina-Porcel, Sabrina Turbant, Daisy Rinaldi, Raquel Sánchez-Valle, Mathieu Barbier, Morwena Latouche, Giovanni Stevanin, Danielle Seilhean, Alexis Brice, Charles Duyckaerts, Isabelle Le Ber
Institutions: Centre National de la Recherche Scientifique, Inserm, Sorbonne Université, Pitié-Salpêtrière Hospital, Institut du Cerveau, Université Pierre-et-Marie-Curie, École Pratique des Hautes Études, Université Paris Sciences et Lettres, Assistance Publique – Hôpitaux de Paris, Hospital Clínic de Barcelona, Consorci Institut D'Investigacions Biomediques August Pi I Sunyer
Language: English
Subfield: Cellular and Molecular Neuroscience
Field: Neuroscience
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $1,304
Funders: Fondation pour l'Aide à la Recherche sur la Sclérose en Plaques, European Commission, Agence Nationale de la Recherche, Assistance Publique - Hôpitaux de Paris, Universität Wien, China Scholarship Council, Chinese Academy of Agricultural Sciences, Centre Hospitalier Régional Universitaire de Montpellier, Medizinische Universität Wien, Association France Parkinson, Centre Hospitalier Universitaire de Rennes, FP7 Ideas: European Research Council
OpenAlex ID: W2807177219