HPCA Confirmed as a Genetic Cause of DYT2-Like Dystonia Phenotype

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dc.contributor.author Atasu, Burcu
dc.contributor.author Hauser, Ann-Kathrin
dc.contributor.author Simón-Sánchez, Javier
dc.contributor.author Heutink, Peter
dc.contributor.author Gasser, Thomas
dc.contributor.author Lohmann, Ebba
dc.date.accessioned 2019-08-16T08:10:24Z
dc.date.available 2019-08-16T08:10:24Z
dc.date.issued 2018
dc.identifier.issn 1531-8257
dc.identifier.uri http://hdl.handle.net/10900/91564
dc.language.iso en en
dc.publisher Wiley de_DE
dc.relation.uri http://dx.doi.org/10.1002/mds.27442
dc.subject.ddc 610 de_DE
dc.title HPCA Confirmed as a Genetic Cause of DYT2-Like Dystonia Phenotype de_DE
dc.type Artikel de_DE
utue.quellen.id 20190321153956_01600
utue.publikation.seiten 1354-1358 de_DE
utue.personen.roh Atasu, Burcu
utue.personen.roh Hanagasi, Hasmet
utue.personen.roh Bilgic, Basar
utue.personen.roh Pak, Meltem
utue.personen.roh Erginel-Unaltuna, Nihan
utue.personen.roh Hauser, Ann-Kathrin
utue.personen.roh Guven, Gamze
utue.personen.roh Simon-Sanchez, Javier
utue.personen.roh Heutink, Peter
utue.personen.roh Gasser, Thomas
utue.personen.roh Lohmann, Ebba
dcterms.isPartOf.ZSTitelID Movement Disorders de_DE
dcterms.isPartOf.ZS-Issue 8 de_DE
dcterms.isPartOf.ZS-Volume 33 de_DE
utue.fakultaet Sonstige
utue.fakultaet 04 Medizinische Fakultät


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