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dc.creatorCardenas, Ana M
dc.creatorGonzalez-Jamett, Arlek M
dc.creatorCea, Luis A
dc.creatorBevilacqua, Jorge A
dc.creatorCaviedes, Pablo
dc.date.accessioned2018-12-07T13:33:44Z
dc.date.available2018-12-07T13:33:44Z
dc.date.issued2016
dc.identifier.urihttp://hdl.handle.net/10533/232692
dc.description.abstractMutations in the dysferlin gene are linked to a group of muscular dystrophies known as dysferlinopathies. These myopathies are characterized by progressive atrophy. Studies in muscle tissue from dysferlinopathy patients or dysferlin-deficient mice point o
dc.language.isoeng
dc.relation.urihttps://www.sciencedirect.com/science/article/pii/S0014488616301911?via%3Dihub
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 Chile
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.titleDysferlin function in skeletal muscle: possible pathological mechanisms and therapeutical targets in dysferlinopathies
dc.typeArticulo
dc.description.conicytinstrumentRegular
dc.identifier.folio1151383
dc.description.conicytprogramFONDECYT
dc.relation.contesthandle/10533/111557
dc.rights.driverinfo:eu-repo/semantics/openAccess
dc.title.journalExperimental Neurology
dc.type.driverinfo:eu-repo/semantics/article
dc.relation.instrumenthandle/10533/111541
dc.relation.programhandle/10533/108045
dc.description.shortconicytprogramFONDECYT
dc.date.annoconcurso2015
dc.type.openaireinfo:eu-repo/semantics/publishedVersion


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