TY  - JOUR
AU  - Corral-Juan, Marc
AU  - Serrano-Munuera, Carmen
AU  - Rabano, Alberto
AU  - Cota-Gonzalez, Daniel
AU  - Segarra-Roca, Anna
AU  - Ispierto, Lourdes
AU  - Cano-Orgaz, Antonio Tomas
AU  - Adarmes, Astrid D
AU  - Meéndez-Del-Barrio, Carlota
AU  - Jesus, Silvia
AU  - Mir, Pablo
AU  - Volpini, Victor
AU  - Alvarez-Ramo, Ramiro
AU  - Sanchez, Ivelisse
AU  - Matilla-Dueñas, Antoni
PY  - 2018
DO  - 10.1093/brain/awy137
UR  - http://hdl.handle.net/10668/12638
T2  - Brain : a journal of neurology
AB  - The autosomal dominant spinocerebellar ataxias (SCAs) consist of a highly heterogeneous group of rare movement disorders characterized by progressive cerebellar ataxia variably associated with ophthalmoplegia, pyramidal and extrapyramidal signs,...
LA  - en
PB  - Oxford University Press
KW  - ATTTC pentanucleotide mutation
KW  - DAB1
KW  - Purkinje cells
KW  - reelin
KW  - spinocerebellar ataxia 37
KW  - Adaptor Proteins, Signal Transducing
KW  - Adult
KW  - Ataxia
KW  - Cell Adhesion Molecules, Neuronal
KW  - Cerebellum
KW  - Extracellular Matrix Proteins
KW  - Female
KW  - Humans
KW  - Male
KW  - Microsatellite Repeats
KW  - Mutation
KW  - Nerve Tissue Proteins
KW  - Nervous System Diseases
KW  - Neuropathology
KW  - Pedigree
KW  - Purkinje Cells
KW  - Reelin Protein
KW  - Serine Endopeptidases
KW  - Spinocerebellar Ataxias
KW  - Spinocerebellar Degenerations
TI  - Clinical, genetic and neuropathological characterization of spinocerebellar ataxia type 37.
TY  - research article
VL  - 141
ER  -