Clinically variable nemaline myopathy in a three-generation family caused by mutation of the skeletal muscle alpha-actin gene

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dc.contributor.authorVilma-Lotta Lehtokari
dc.contributor.authorMaria Gardberg
dc.contributor.authorKatarina Pelin
dc.contributor.authorCarina Wallgren-Pettersson
dc.contributor.organizationfi=biolääketieteen laitos|en=Institute of Biomedicine|
dc.contributor.organization-code1.2.246.10.2458963.20.77952289591
dc.converis.publication-id30792900
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/30792900
dc.date.accessioned2022-10-28T13:52:52Z
dc.date.available2022-10-28T13:52:52Z
dc.format.pagerange323
dc.format.pagerange326
dc.identifier.eissn1873-2364
dc.identifier.jour-issn0960-8966
dc.identifier.olddbid184934
dc.identifier.oldhandle10024/168028
dc.identifier.urihttps://www.utupub.fi/handle/11111/41868
dc.identifier.urnURN:NBN:fi-fe2021042719023
dc.language.isoen
dc.okm.affiliatedauthorGardberg, Maria
dc.okm.discipline3121 Internal medicineen_GB
dc.okm.discipline3121 Sisätauditfi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherElsevier Ltd
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.doi10.1016/j.nmd.2017.12.009
dc.relation.ispartofjournalNeuromuscular Disorders
dc.relation.issue4
dc.relation.volume28
dc.source.identifierhttps://www.utupub.fi/handle/10024/168028
dc.titleClinically variable nemaline myopathy in a three-generation family caused by mutation of the skeletal muscle alpha-actin gene
dc.year.issued2018

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