Show simple item record

dc.contributor.authorBeck, M.
dc.contributor.authorAguti, S.
dc.contributor.authorAla, P.
dc.contributor.authorRichard-Loendt, A.
dc.contributor.authorChambers, D.
dc.contributor.authorScaglioni, D.
dc.contributor.authorArdicli, D.
dc.contributor.authorFeng, L.
dc.contributor.authorMein, R.
dc.contributor.authorZhou, H.
dc.contributor.authorSewry, C.
dc.contributor.authorSarkozy, A.
dc.contributor.authorTorelli, S.
dc.contributor.authorMuntoni, F.
dc.contributor.authorPhadke, R.
dc.date.accessioned2021-06-03T05:42:52Z
dc.date.available2021-06-03T05:42:52Z
dc.date.issued2019
dc.identifier.issn0960-8966
dc.identifier.urihttp://dx.doi.org/10.1016/j.nmd.2019.06.549
dc.identifier.urihttp://hdl.handle.net/11655/24091
dc.language.isoen
dc.relation.isversionof10.1016/j.nmd.2019.06.549
dc.rightsAttribution 4.0 United States
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleA Novel In Situ Hybridisation (Ish) Assay Mapping The In-Frame Pseudoexon 11 (Pe11) Expression In Cultured Dermal Fibroblasts (Cdf) And Skeletal Muscle In Patients With Severe Collagen Vi Disease Due To A Deep Intronic Mutation In Col6A1
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalNeuromuscular Disorders
dc.contributor.departmentNöroloji
dc.identifier.volume29
dc.identifier.issue1
dc.description.indexWoS


Files in this item

This item appears in the following Collection(s)

Show simple item record

Attribution 4.0 United States
Except where otherwise noted, this item's license is described as Attribution 4.0 United States