dc.date.accessioned2022-06-25T20:36:43Z
dc.date.available2022-06-25T20:36:43Z
dc.date.created2022-06-25T20:36:43Z
dc.date.issued2022
dc.identifierhttps://hdl.handle.net/20.500.12866/11890
dc.identifierhttps://doi.org/10.1002/mds.29046
dc.description.abstractAutosomal 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.languageeng
dc.publisherWiley
dc.relationMovement Disorders
dc.relation1531-8257
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/4.0/deed.es
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectLetter
dc.subjectAutosomal Recessive Cerebellar Ataxias
dc.subjectSouth America
dc.subjectMulticenter Study
dc.titleAutosomal Recessive Cerebellar Ataxias in South America: A Multicenter Study of 1338 Patients
dc.typeinfo:eu-repo/semantics/article


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