dc.date.accessioned | 2022-06-25T20:36:43Z | |
dc.date.available | 2022-06-25T20:36:43Z | |
dc.date.created | 2022-06-25T20:36:43Z | |
dc.date.issued | 2022 | |
dc.identifier | https://hdl.handle.net/20.500.12866/11890 | |
dc.identifier | https://doi.org/10.1002/mds.29046 | |
dc.description.abstract | Autosomal recessive cerebellar ataxias (ARCAs) comprisecomplex genetic ataxia disorders with variable central andperipheral nervous system involvement and systemic changes.They can overlap with other conditions such as hereditary spas-tic paraplegia, inborn errors of metabolism, and genetic enceph-alopathies.1While usually starting in childhood or youngadulthood, late adult-onset may occur. The advanced applica-tion of next-generation sequencing has allowed the moleculardefinition of many previously undetermined ARCAs in the lastdecade, including many new ARCA genes. | |
dc.language | eng | |
dc.publisher | Wiley | |
dc.relation | Movement Disorders | |
dc.relation | 1531-8257 | |
dc.rights | https://creativecommons.org/licenses/by-nc-nd/4.0/deed.es | |
dc.rights | info:eu-repo/semantics/restrictedAccess | |
dc.subject | Letter | |
dc.subject | Autosomal Recessive Cerebellar Ataxias | |
dc.subject | South America | |
dc.subject | Multicenter Study | |
dc.title | Autosomal Recessive Cerebellar Ataxias in South America: A Multicenter Study of 1338 Patients | |
dc.type | info:eu-repo/semantics/article | |