A Recurrent Mutation in KCNA2 as a Novel Cause of Hereditary Spastic Paraplegia and Ataxia

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dc.contributor.author Hedrich, Ulrike B. S.
dc.contributor.author Schubert, Julian
dc.contributor.author Synofzik, Matthis Benjamin
dc.contributor.author Lerche, Holger
dc.contributor.author Karle, Kathrin Nora
dc.contributor.author Schöls, Ludger
dc.contributor.author Schüle-Freyer, Rebecca
dc.date.accessioned 2018-11-29T13:39:55Z
dc.date.available 2018-11-29T13:39:55Z
dc.date.issued 2016
dc.identifier.issn 1531-8249
dc.identifier.uri http://hdl.handle.net/10900/85082
dc.language.iso en de_DE
dc.publisher Wiley - Blackwell de_DE
dc.relation.uri http://dx.doi.org/10.1002/ana.24762 de_DE
dc.rights info:eu-repo/semantics/closedAccess
dc.subject.ddc 570 de_DE
dc.subject.ddc 610 de_DE
dc.title A Recurrent Mutation in KCNA2 as a Novel Cause of Hereditary Spastic Paraplegia and Ataxia de_DE
dc.type Artikel de_DE
utue.quellen.id 20180405102126_00806
utue.publikation.seiten 638-642 de_DE
utue.personen.roh Helbig, Katherine L.
utue.personen.roh Hedrich, Ulrike B. S.
utue.personen.roh Shinde, Deepali N.
utue.personen.roh Krey, Ilona
utue.personen.roh Teichmann, Anne-Christin
utue.personen.roh Hentschel, Julia
utue.personen.roh Schubert, Julian
utue.personen.roh Chamberlin, Adam C.
utue.personen.roh Huether, Robert
utue.personen.roh Lu, Hsiao-Mei
utue.personen.roh Alcaraz, Wendy A.
utue.personen.roh Tang, Sha
utue.personen.roh Jungbluth, Chelsy
utue.personen.roh Dugan, Sarah L.
utue.personen.roh Vainionpaa, Leena
utue.personen.roh Karle, Kathrin N.
utue.personen.roh Synofzik, Matthis
utue.personen.roh Lehesjoki, Anna-Elina
utue.personen.roh Helbig, Ingo
utue.personen.roh Lerche, Holger
utue.personen.roh Lemke, Johannes R.
utue.personen.roh Schöls, Ludger
utue.personen.roh Schüle-Freyer, Rebecca
dcterms.isPartOf.ZSTitelID Annals of Neurology de_DE
dcterms.isPartOf.ZS-Issue 4 de_DE
dcterms.isPartOf.ZS-Volume 80 de_DE
utue.fakultaet 04 Medizinische Fakultät de_DE


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