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dc.contributor.authorØstern, Rune André Helland
dc.contributor.authorFagerheim, Toril
dc.contributor.authorHjellnes, Helene
dc.contributor.authorNygård, Bjørn
dc.contributor.authorMellgren, Svein Ivar
dc.contributor.authorNilssen, Øivind
dc.date.accessioned2015-03-13T11:26:19Z
dc.date.available2015-03-13T11:26:19Z
dc.date.issued2014
dc.identifier.citationBMC Medical Genetics 2014, 15:12en_US
dc.identifier.cristinIDFRIDAID 1128672
dc.identifier.doi10.1186/1471-2350-15-12
dc.identifier.issn1471-2350
dc.identifier.urihttps://hdl.handle.net/10037/7485
dc.identifier.urnURN:NBN:no-uit_munin_7075
dc.language.isoengen_US
dc.publisherBioMed Centralen_US
dc.rights.accessRightsopenAccess
dc.subjectVDP::714en_US
dc.subjectVDP::752en_US
dc.titleSegregation analysis in families with Charcot-Marie-Tooth disease allows reclassification of putative disease causing mutationsen_US
dc.typeJournal articleen_US
dc.typeTidsskriftartikkelen_US
dc.typePeer revieweden_US


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