| dc.contributor.author | Manrique, Leire | |
| dc.contributor.author | Sánchez-Rodríguez, Antonio | |
| dc.contributor.author | Pelayo Negro, Ana. L. | |
| dc.contributor.author | Corral-Juan, Marc | |
| dc.contributor.author | Matilla-Dueñas, Antoni | |
| dc.contributor.author | Infante Ceberio, Jon | |
| dc.contributor.other | Universidad de Cantabria | es_ES |
| dc.date.accessioned | 2022-02-22T19:08:25Z | |
| dc.date.available | 2022-05-19T23:01:56Z | |
| dc.date.issued | 2021-05-19 | |
| dc.identifier.issn | 0885-3185 | |
| dc.identifier.issn | 1531-8257 | |
| dc.identifier.uri | http://hdl.handle.net/10902/24021 | |
| dc.format.extent | 3 p. | es_ES |
| dc.language.iso | eng | es_ES |
| dc.publisher | John Wiley and Sons Inc. | es_ES |
| dc.rights | This is the peer reviewed version of the following article: [Manrique, L., Sánchez-Rodríguez, A., Pelayo-Negro, A.L., Corral-Juan, M., Matilla-Dueñas, A. and Infante, J. (2021), Ataxia and Action Myoclonus Related to Novel Mutations in ATP13A2 Gene. Mov Disord Clin Pract, 8: 969-971], which has been published in final form at [https://doi.org/10.1002/mdc3.13260]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving. | es_ES |
| dc.source | Movement Disorders, 2021; Volume8, Issue6; Pages 969-971 | es_ES |
| dc.subject.other | Ataxia | es_ES |
| dc.subject.other | Myoclonus | es_ES |
| dc.subject.other | ATP13A2 | es_ES |
| dc.subject.other | Mutation | es_ES |
| dc.subject.other | Kufor-Rakeb | es_ES |
| dc.title | Ataxia and Action Myoclonus Related to Novel Mutations in ATP13A2 Gene | es_ES |
| dc.type | info:eu-repo/semantics/article | es_ES |
| dc.relation.publisherVersion | https://doi.org/10.1002/mdc3.13260 | es_ES |
| dc.rights.accessRights | openAccess | es_ES |
| dc.identifier.DOI | 10.1002/mdc3.13260 | |
| dc.type.version | acceptedVersion | es_ES |
