Publication
Downbeat Nystagmus in Episodic Ataxia Type 1 Associated with a Novel KCNA1 Mutation
| dc.contributor.author | Jorge, A | |
| dc.contributor.author | Melancia, D | |
| dc.contributor.author | Figueiredo, C | |
| dc.contributor.author | Galego, O | |
| dc.contributor.author | Oliveira, J | |
| dc.contributor.author | Martins, AI | |
| dc.contributor.author | Lemos, J | |
| dc.date.accessioned | 2023-05-04T11:28:03Z | |
| dc.date.available | 2023-05-04T11:28:03Z | |
| dc.date.issued | 2022 | |
| dc.description.version | info:eu-repo/semantics/publishedVersion | pt_PT |
| dc.identifier.citation | Mov Disord . 2022 Feb;37(2):430-432 | pt_PT |
| dc.identifier.doi | 10.1002/mds.28843 | pt_PT |
| dc.identifier.uri | http://hdl.handle.net/10400.17/4505 | |
| dc.language.iso | eng | pt_PT |
| dc.peerreviewed | yes | pt_PT |
| dc.publisher | Wiley | pt_PT |
| dc.subject | Ataxia / complications | pt_PT |
| dc.subject | Ataxia / genetics | pt_PT |
| dc.subject | Humans | pt_PT |
| dc.subject | Kv1.1 Potassium Channel / genetics | pt_PT |
| dc.subject | Mutation / genetics | pt_PT |
| dc.subject | Myokymia* | pt_PT |
| dc.subject | Nystagmus, Pathologic* / genetics | pt_PT |
| dc.subject | HSAC NEU | pt_PT |
| dc.title | Downbeat Nystagmus in Episodic Ataxia Type 1 Associated with a Novel KCNA1 Mutation | pt_PT |
| dc.type | journal article | |
| dspace.entity.type | Publication | |
| oaire.citation.endPage | 432 | pt_PT |
| oaire.citation.issue | 2 | pt_PT |
| oaire.citation.startPage | 430 | pt_PT |
| oaire.citation.title | Movement Disorders | pt_PT |
| oaire.citation.volume | 37 | pt_PT |
| rcaap.rights | openAccess | pt_PT |
| rcaap.type | article | pt_PT |