dc.date.accessioned2020-03-11T20:37:49Z
dc.date.accessioned2022-10-18T23:06:57Z
dc.date.available2020-03-11T20:37:49Z
dc.date.available2022-10-18T23:06:57Z
dc.date.created2020-03-11T20:37:49Z
dc.date.issued2012
dc.identifierhttp://hdl.handle.net/10533/241421
dc.identifier15090007
dc.identifierWOS:000299986600006
dc.identifierno scielo
dc.identifiereid=2-s2.0-83155178547
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4472760
dc.description.abstractNiemann-Pick C disease (NPC) is a neuro-visceral lysosomal storage disorder mainly caused by genetic defects in the NPC1 gene. As a result of loss of NPC1 function large quantities of free cholesterol and other lipids accumulate within late endosomes and
dc.languageeng
dc.relationhttps://doi.org/10.1016/j.bbadis.2011.11.009
dc.relation10.1016/j.bbadis.2011.11.009
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.titleLysosomal vitamin E accumulation in Niemann-Pick type C disease.
dc.typeArticulo


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