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Ullrich Congenital Muscular Dystrophy In A Boy With 21Q22.3 Deletion: A Revisited Diagnosis

dc.contributor.authorKiper, P. Simsek
dc.contributor.authorOguz, S.
dc.contributor.authorUtine, G.
dc.contributor.authorKasifoglu, M.
dc.contributor.authorHaliloglu, G.
dc.date.accessioned2021-06-02T10:39:25Z
dc.date.available2021-06-02T10:39:25Z
dc.date.issued2019
dc.identifier.issn0960-8966
dc.identifier.urihttp://dx.doi.org/10.1016/j.nmd.2019.06.585
dc.identifier.urihttp://hdl.handle.net/11655/23760
dc.language.isoen
dc.relation.isversionof10.1016/j.nmd.2019.06.585
dc.rightsAttribution 4.0 United States
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleUllrich Congenital Muscular Dystrophy In A Boy With 21Q22.3 Deletion: A Revisited Diagnosis
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalNeuromuscular Disorders
dc.contributor.departmentÇocuk Sağlığı ve Hastalıkları
dc.identifier.volume29
dc.identifier.issue1
dc.description.indexWoS


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