Autosomal dominant optic atrophy: A novel treatment for OPA1 splice defects using U1 snRNA adaption

Jueschke, Christoph; Klopstock, Thomas; Catarino, Claudia B.; Owczarek-Lipska, Marta; Wissinger, Bernd; Neidhardt, John

dc.contributor.author	Wissinger, Bernd
dc.date.accessioned	2022-07-04T06:34:32Z
dc.date.available	2022-07-04T06:34:32Z
dc.date.issued	2021
dc.identifier.issn	2162-2531
dc.identifier.uri	http://hdl.handle.net/10900/128964
dc.language.iso	en	de_DE
dc.publisher	Cambridge	de_DE
dc.relation.uri	http://dx.doi.org/10.1016/j.omtn.2021.10.019	de_DE
dc.subject.ddc	610	de_DE
dc.title	Autosomal dominant optic atrophy: A novel treatment for OPA1 splice defects using U1 snRNA adaption	de_DE
dc.type	Article	de_DE
utue.quellen.id	20220404000000_00519
utue.publikation.seiten	1186-1197	de_DE
utue.personen.roh	Jueschke, Christoph
utue.personen.roh	Klopstock, Thomas
utue.personen.roh	Catarino, Claudia B.
utue.personen.roh	Owczarek-Lipska, Marta
utue.personen.roh	Wissinger, Bernd
utue.personen.roh	Neidhardt, John
dcterms.isPartOf.ZSTitelID	Molecular Therapy - Nucleic Acids	de_DE
dcterms.isPartOf.ZS-Volume	26	de_DE
utue.fakultaet	04 Medizinische Fakultät	de_DE