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

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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