Mutations in MT-ATP6 are a frequent cause of adult-onset spinocerebellar ataxia

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dc.contributor.authorNolte, Dagmar
dc.contributor.authorKang, Jun-Suk
dc.contributor.authorHofmann, Amrei
dc.contributor.authorSchwaab, Eva
dc.contributor.authorKrämer, Heidrun H.
dc.contributor.authorMüller, Ulrich
dc.date.accessioned2022-11-16T14:51:12Z
dc.date.available2022-11-16T14:51:12Z
dc.date.issued2021
dc.identifier.urihttps://jlupub.ub.uni-giessen.de//handle/jlupub/8597
dc.identifier.urihttp://dx.doi.org/10.22029/jlupub-7985
dc.language.isoen
dc.rightsNamensnennung 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subject.ddcddc:610
dc.titleMutations in MT-ATP6 are a frequent cause of adult-onset spinocerebellar ataxia
dc.typearticle
local.affiliationFB 11 - Medizin
local.source.epage4873
local.source.journaltitleJournal of neurology
local.source.spage4866
local.source.urihttps://doi.org/10.1007/s00415-021-10607-5
local.source.volume268

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