A Severe Dementia Syndrome Caused by Intron Retention and Cryptic Splice Site Activation in STUB1 and Exacerbated by TBP Repeat Expansions

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dc.contributor.authorReis, Marien Colleen
dc.contributor.authorPatrun, Julia
dc.contributor.authorAckl, Nibal
dc.contributor.authorWinter, Pia
dc.contributor.authorScheifele, Maximilian
dc.contributor.authorDanek, Adrian
dc.contributor.authorNolte, Dagmar
dc.date.accessioned2022-08-18T06:12:41Z
dc.date.available2022-08-18T06:12:41Z
dc.date.issued2022
dc.identifier.urihttps://jlupub.ub.uni-giessen.de//handle/jlupub/6539
dc.identifier.urihttp://dx.doi.org/10.22029/jlupub-5990
dc.language.isoen
dc.rightsNamensnennung 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subject.ddcddc:610
dc.titleA Severe Dementia Syndrome Caused by Intron Retention and Cryptic Splice Site Activation in STUB1 and Exacerbated by TBP Repeat Expansions
dc.typearticle
local.affiliationFB 11 - Medizin
local.source.articlenumber878236
local.source.epage11
local.source.journaltitleFrontiers in molecular neuroscience
local.source.spage1
local.source.urihttps://doi.org/10.3389/fnmol.2022.878236
local.source.volume15

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