Mutations at a split codon in the GTPase-encoding domain of OPA1 cause dominant optic atrophy through different molecular mechanisms

Weisschuh, Nicole; Marino, Valerio; Schaeferhoff, Karin; Richter, Paul; Park, Joohyun; Haack, Tobias B.; Dell'Orco, Daniele

dc.contributor.author	Weisschuh, Nicole
dc.contributor.author	Richter, Paul
dc.contributor.author	Park, Joohyun
dc.contributor.author	Schäferhoff, Karin
dc.contributor.author	Haack, Tobias
dc.date.accessioned	2023-04-25T09:19:02Z
dc.date.available	2023-04-25T09:19:02Z
dc.date.issued	2022
dc.identifier.issn	0964-6906
dc.identifier.uri	http://hdl.handle.net/10900/139603
dc.language.iso	en	de_DE
dc.publisher	Oxford Univ Press	de_DE
dc.relation.uri	http://dx.doi.org/10.1093/hmg/ddab286	de_DE
dc.subject.ddc	570	de_DE
dc.subject.ddc	610	de_DE
dc.title	Mutations at a split codon in the GTPase-encoding domain of OPA1 cause dominant optic atrophy through different molecular mechanisms	de_DE
dc.type	Article	de_DE
utue.quellen.id	20220728000000_02884
utue.publikation.seiten	761-774	de_DE
utue.personen.roh	Weisschuh, Nicole
utue.personen.roh	Marino, Valerio
utue.personen.roh	Schaeferhoff, Karin
utue.personen.roh	Richter, Paul
utue.personen.roh	Park, Joohyun
utue.personen.roh	Haack, Tobias B.
utue.personen.roh	Dell'Orco, Daniele
dcterms.isPartOf.ZSTitelID	Human Molecular Genetics	de_DE
dcterms.isPartOf.ZS-Issue	5	de_DE
dcterms.isPartOf.ZS-Volume	31	de_DE
utue.fakultaet	04 Medizinische Fakultät	de_DE