AAV8-based gene replacement therapy for hereditary spastic paraplegia type 5

dc.contributor.author	Wiora, Linus
dc.contributor.author	Kraft, Melanie
dc.contributor.author	Hauser, Stefan
dc.contributor.author	Schöls, Ludger
dc.date.accessioned	2026-06-02T10:15:27Z
dc.date.available	2026-06-02T10:15:27Z
dc.date.issued	2025
dc.identifier.issn	2329-0501
dc.identifier.uri	http://hdl.handle.net/10900/180208
dc.language.iso	en	de_DE
dc.publisher	Cambridge : Cell Press	de_DE
dc.relation.uri	http://dx.doi.org/10.1016/j.omtm.2025.101531	de_DE
dc.subject.ddc	610	de_DE
dc.title	AAV8-based gene replacement therapy for hereditary spastic paraplegia type 5	de_DE
dc.type	Article	de_DE
utue.quellen.id	20251118000000_00727
utue.personen.roh	Wiora, Linus
utue.personen.roh	Yuan, Qinggong
utue.personen.roh	Hook, Sebastian
utue.personen.roh	Kraft, Melanie
utue.personen.roh	Bjoerkhem, Ingemar
utue.personen.roh	Ott, Michael
utue.personen.roh	Hauser, Stefan
utue.personen.roh	Schoels, Ludger
dcterms.isPartOf.ZSTitelID	Molecular Therapy Methods & Clinical Development	de_DE
dcterms.isPartOf.ZS-Issue	Article 101531	de_DE
dcterms.isPartOf.ZS-Volume	33 (3)	de_DE
utue.fakultaet	04 Medizinische Fakultät	de_DE

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