Homozygous TBC1 domain-containing kinase (TBCK) mutation causes a novel lysosomal storage disease - a new type of neuronal ceroid lipofuscinosis (CLN15)?

Beck-Woedl, Stefanie; Harzer, Klaus; Sturm, Marc; Buchert, Rebecca; Riess, Olaf; Mennel, Hans-Dieter; Latta, Elisabeth; Pagenstecher, Axel; Keber, Ursula

dc.contributor.author	Harzer, Klaus
dc.contributor.author	Sturm, Marc
dc.contributor.author	Buchert, Rebecca
dc.contributor.author	Beck-Wödl, Stefanie
dc.contributor.author	Rieß, Olaf
dc.date.accessioned	2019-06-19T15:05:50Z
dc.date.available	2019-06-19T15:05:50Z
dc.date.issued	2018
dc.identifier.issn	2051-5960
dc.identifier.uri	http://hdl.handle.net/10900/89759
dc.language.iso	en	de_DE
dc.publisher	Bmc	de_DE
dc.relation.uri	http://dx.doi.org/10.1186/s40478-018-0646-6	de_DE
dc.rights	info:eu-repo/semantics/closedAccess
dc.subject.ddc	570	de_DE
dc.subject.ddc	610	de_DE
dc.title	Homozygous TBC1 domain-containing kinase (TBCK) mutation causes a novel lysosomal storage disease - a new type of neuronal ceroid lipofuscinosis (CLN15)?	de_DE
dc.type	Article	de_DE
utue.quellen.id	20190321153956_00003
utue.personen.roh	Beck-Woedl, Stefanie
utue.personen.roh	Harzer, Klaus
utue.personen.roh	Sturm, Marc
utue.personen.roh	Buchert, Rebecca
utue.personen.roh	Riess, Olaf
utue.personen.roh	Mennel, Hans-Dieter
utue.personen.roh	Latta, Elisabeth
utue.personen.roh	Pagenstecher, Axel
utue.personen.roh	Keber, Ursula
dcterms.isPartOf.ZSTitelID	Acta Neuropathologica Communications	de_DE
dcterms.isPartOf.ZS-Issue	Article 145	de_DE
dcterms.isPartOf.ZS-Volume	6	de_DE
utue.fakultaet	04 Medizinische Fakultät	de_DE