Evolving neuromuscular phenotype in a patient with a heterozygous CHCHD10 p.G66V mutation

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dc.contributor.authorJokela Manu
dc.contributor.authorJoutsa Juho
dc.contributor.authorUdd Bjarne
dc.contributor.organizationfi=kliiniset neurotieteet|en=Clinical Neurosciences|
dc.contributor.organization-code1.2.246.10.2458963.20.74845969893
dc.contributor.organization-code2607314
dc.converis.publication-id28351663
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/28351663
dc.date.accessioned2022-10-28T12:19:17Z
dc.date.available2022-10-28T12:19:17Z
dc.format.pagerange1461
dc.format.pagerange1462
dc.identifier.jour-issn0340-5354
dc.identifier.olddbid175820
dc.identifier.oldhandle10024/158914
dc.identifier.urihttps://www.utupub.fi/handle/11111/45879
dc.identifier.urnURN:NBN:fi-fe2021042717879
dc.language.isoen
dc.okm.affiliatedauthorJokela, Manu
dc.okm.affiliatedauthorJoutsa, Juho
dc.okm.discipline3124 Neurology and psychiatryen_GB
dc.okm.discipline3124 Neurologia ja psykiatriafi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeB1 Scientific Journal
dc.relation.doi10.1007/s00415-016-8134-z
dc.relation.ispartofjournalJournal of Neurology
dc.relation.issue7
dc.relation.volume263
dc.source.identifierhttps://www.utupub.fi/handle/10024/158914
dc.titleEvolving neuromuscular phenotype in a patient with a heterozygous CHCHD10 p.G66V mutation
dc.year.issued2016

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