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Paper Details

Heterozygous <i>STUB1</i> mutation causes familial ataxia with cognitive affective syndrome (SCA48).
Neurology
66
2018
Author NameAffiliation
Sergi BeltranLaboratori Clinic Territorial de Girona (M.O.), Institute of Diagnostic Imaging (IDI), University Hospital "Dr. Josep Trueta," Hospital de Santa Caterina, Parc Hospitalari Marti i Julia Group of Investigation in Neurodegeneration and Neuroinflammation (D.G., Institut d'Investigacio Biomedica de Girona Dr. Josep Trueta (IDIBGI), University of Girona Neurogenetics Laboratory, Center for Applied Medical Research, University of Navarra, Hospital Universitario de Burgos (HUBU) CIBERNED, Instituto de Salud Carlos III, Institut d'Investigacio Biomedica de Bellvitge (IDIBELL), L'Hospitalet de Llobregat, Center for Genomic Regulation, Barcelona Institute of Science and Technology (BIST) Universitat Pompeu Fabra (UPF) (R.T., Barcelona National Bioinformatics Institute (R.T.), Madrid Clinical Psychology (L.F.), Hospital de Dia de Malalties Neurodegeneratives, Hospital de Santa Caterina, Parc Hospitalari Marti i Julia, University Hospital Mutua de Terrassa
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