Increased copper levels in in vitro and in vivo models of Niemann-Pick C disease

dc.date.accessioned2020-03-11T20:37:56Z
dc.date.accessioned2022-10-18T23:07:11Z
dc.date.available2020-03-11T20:37:56Z
dc.date.available2022-10-18T23:07:11Z
dc.date.created2020-03-11T20:37:56Z
dc.date.issued2012
dc.identifierhttp://hdl.handle.net/10533/241453
dc.identifier15090007
dc.identifierWOS:000305731100013
dc.identifierno scielo
dc.identifiereid=2-s2.0-84864951534
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4472792
dc.description.abstractNiemann-Pick type C disease (NPC) is a hereditary neurovisceral atypical lipid storage disorder produced by mutations in the NPC1 and NPC2 genes. The disease is characterized by unesterified cholesterol accumulation in late endosomal/lysosomal compartment
dc.languageeng
dc.relationhttps://doi.org/10.1007/s10534-012-9546-6
dc.relation10.1007/s10534-012-9546-6
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 Chile
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.titleIncreased copper levels in in vitro and in vivo models of Niemann-Pick C disease
dc.typeArticulo


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