High creatine kinase levels and white matter changes : Clinical and genetic spectrum of congenital muscular dystrophies with laminin alpha-2 deficiency

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dc.contributor.authorBeytía Reyes, María de Los Ángeles
dc.contributor.authorDekomien, G.
dc.contributor.authorHoffjan, S.
dc.contributor.authorHaug, V.
dc.contributor.authorAnastasopoulos, C.
dc.contributor.authorKirschner, J.
dc.date.accessioned2020-10-02T00:43:50Z
dc.date.available2020-10-02T00:43:50Z
dc.date.issued2014
dc.format.extent5 páginas
dc.fuente.origenConveris
dc.identifier.doi10.1016/j.mcp.2013.11.002
dc.identifier.issn0890-8508
dc.identifier.issn1096-1194
dc.identifier.urihttps://doi.org/10.1016/j.mcp.2013.11.002
dc.identifier.urihttps://repositorio.uc.cl/handle/11534/46587
dc.issue.numeroNo. 4
dc.language.isoen
dc.pagina.final122
dc.pagina.inicio118
dc.revistaMolecular and Cellular Probeses_ES
dc.titleHigh creatine kinase levels and white matter changes : Clinical and genetic spectrum of congenital muscular dystrophies with laminin alpha-2 deficiencyes_ES
dc.typeartículo
dc.volumenVol. 28
sipa.codpersvinculados1009448
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