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Rapid-onset dystonia-Parkinsonism phenotype consistency for a novel variant of ATP1A3 in patients across 3 global populations

dc.contributor.authorHoshino, Kyokopt_BR
dc.contributor.authorSweadner, Kathleen J.pt_BR
dc.contributor.authorKawarai, Toshitakapt_BR
dc.contributor.authorSaute, Jonas Alex Moralespt_BR
dc.contributor.authorFreitas, Joelpt_BR
dc.contributor.authorDamasio, Joanapt_BR
dc.contributor.authorDonis, Karina Carvalhopt_BR
dc.contributor.authorKimura, Kazuept_BR
dc.contributor.authorFukuda, Hidekipt_BR
dc.contributor.authorHayash, Masaharupt_BR
dc.contributor.authorHiguchi, Tetsuyapt_BR
dc.contributor.authorIkeda, Yoshiopt_BR
dc.contributor.authorOzelius, Laurie J.pt_BR
dc.contributor.authorKaji, Ryujipt_BR
dc.date.accessioned2022-10-27T04:50:32Zpt_BR
dc.date.issued2021pt_BR
dc.identifier.issn2376-7839pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/250428pt_BR
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoengpt_BR
dc.relation.ispartofNeurology : Genetics. [Hagerstown]. Vol. 7, no. 2 (Apr. 2021), e562, 6 p.pt_BR
dc.rightsOpen Accessen
dc.subjectATPase trocadora de sódio-potássiopt_BR
dc.subjectDistoniapt_BR
dc.subjectMutaçãopt_BR
dc.subjectContração muscularpt_BR
dc.titleRapid-onset dystonia-Parkinsonism phenotype consistency for a novel variant of ATP1A3 in patients across 3 global populationspt_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb001151859pt_BR
dc.type.originEstrangeiropt_BR


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