Intronic<i>FGF14</i>GAA repeat expansions are a common cause of ataxia syndromes with neuropathy and bilateral vestibulopathy
David Pellerin(Université de Sherbrooke), Matthis Synofzik(University of Tübingen), Riccardo Curró(University of Pavia), Sara Nagy(University of Basel), Christel Depienne(Essen University Hospital), Mary M. Reilly(University College London), Bernard Brais(Montreal Neurological Institute and Hospital), Dan Rujescu(Medical University of Vienna), Paola Giunti(University College London Hospitals NHS Foundation Trust), Jennifer Faber, Dagmar Timmann(Essen University Hospital), Andreas Traschütz(German Center for Neurodegenerative Diseases), Carlo Wilke(German Center for Neurodegenerative Diseases), Lüdger Schöls(German Center for Neurodegenerative Diseases), Henry Houlden(National Hospital for Neurology and Neurosurgery), José Gazulla(Hospital Universitario Miguel Servet), Mathieu Anheim(Centre National de la Recherche Scientifique), Thomas Wirth(Centre National de la Recherche Scientifique), Marie‐Josée Dicaire(Institute of Human Genetics), Héctor García‐Moreno(University College London Hospitals NHS Foundation Trust), Michael Strupp(Ludwig-Maximilians-Universität München), Andrea Cortese(National Hospital for Neurology and Neurosurgery)
Cited by 45
Related Papers
Large recurrent microdeletions associated with schizophrenia
|Nature|2008|1.8k
Common variants conferring risk of schizophrenia
|Nature|2009|1.7k
Disruption of the neurexin 1 gene is associated with schizophrenia
|Human Molecular Genetics|2008|485
Brain MRI Findings in Severe COVID-19: A Retrospective Observational Study
|Radiology|2020|471