Mutation in the AP4B1 gene cause hereditary spastic paraplegia type 47 (SPG47)

Bauer, Peter; Leshinsky-Silver, Esther; Blumkin, Lubov; Schlipf, Nina; Schroeder, Christopher; Schicks, Julia; Lev, Dorit; Riess, Olaf; Lerman-Sagie, Tally; Schoels, Ludger

dc.contributor.author	Bauer, Peter
dc.contributor.author	Schlipf, Nina Ariane
dc.contributor.author	Schicks, Julia
dc.contributor.author	Rieß, Olaf
dc.contributor.author	Schroeder, Christopher
dc.contributor.author	Schöls, Ludger
dc.date.accessioned	2014-05-27T15:27:59Z
dc.date.available	2014-05-27T15:27:59Z
dc.date.issued	2012
dc.identifier.issn	1364-6745
dc.identifier.uri	http://hdl.handle.net/10900/53197
dc.language.iso	en	de_DE
dc.publisher	Springer	de_DE
dc.relation.uri	http://dx.doi.org/10.1007/s10048-012-0314-0	de_DE
dc.rights	info:eu-repo/semantics/closedAccess
dc.subject.ddc	570	de_DE
dc.subject.ddc	610	de_DE
dc.title	Mutation in the AP4B1 gene cause hereditary spastic paraplegia type 47 (SPG47)	de_DE
dc.type	Article	de_DE
utue.quellen.id	20140226071329_03329	de_DE
utue.publikation.seiten	73-76	de_DE
utue.personen.roh	Bauer, Peter
utue.personen.roh	Leshinsky-Silver, Esther
utue.personen.roh	Blumkin, Lubov
utue.personen.roh	Schlipf, Nina
utue.personen.roh	Schroeder, Christopher
utue.personen.roh	Schicks, Julia
utue.personen.roh	Lev, Dorit
utue.personen.roh	Riess, Olaf
utue.personen.roh	Lerman-Sagie, Tally
utue.personen.roh	Schoels, Ludger
dcterms.isPartOf.ZSTitelID	Neurogenetics	de_DE
dcterms.isPartOf.ZS-Issue	1	de_DE
dcterms.isPartOf.ZS-Volume	13	de_DE
utue.fakultaet	04 Medizinische Fakultät	de_DE