POLG and PEO1 (Twinkle) mutations are infrequent in PSP-like atypical parkinsonism : a preliminary screening study.

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dc.contributor.author Synofzik, Matthis Benjamin
dc.contributor.author Schicks, Julia
dc.contributor.author Srulijes, Karin
dc.contributor.author Schulte, Claudia
dc.contributor.author Schiele, Franziska
dc.contributor.author Berg, Daniela
dc.contributor.author Schöls, Ludger
dc.date.accessioned 2016-04-29T10:00:49Z
dc.date.available 2016-04-29T10:00:49Z
dc.date.issued 2012
dc.identifier.issn 0340-5354
dc.identifier.uri http://hdl.handle.net/10900/69430
dc.language.iso en de_DE
dc.publisher Berlin ; Heidelberg : Springer de_DE
dc.relation.uri http://dx.doi.org/10.1007/s00415-012-6535-1 de_DE
dc.rights info:eu-repo/semantics/closedAccess
dc.subject.ddc 610 de_DE
dc.title POLG and PEO1 (Twinkle) mutations are infrequent in PSP-like atypical parkinsonism : a preliminary screening study. de_DE
dc.type Artikel de_DE
utue.publikation.seiten 2232-2233 de_DE
utue.personen.roh Synofzik, Matthis
utue.personen.roh Schicks, Julia
utue.personen.roh Srulijes, Karin
utue.personen.roh Schulte, Claudia
utue.personen.roh Schiele, Franziska
utue.personen.roh Berg, Daniela
utue.personen.roh Schöls, Ludger
dcterms.isPartOf.ZSTitelID Journal of neurology de_DE
dcterms.isPartOf.ZS-Issue 10 de_DE
dcterms.isPartOf.ZS-Volume 259 de_DE


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