dc.date.accessioned | 2020-03-11T20:37:49Z | |
dc.date.accessioned | 2022-10-18T23:06:57Z | |
dc.date.available | 2020-03-11T20:37:49Z | |
dc.date.available | 2022-10-18T23:06:57Z | |
dc.date.created | 2020-03-11T20:37:49Z | |
dc.date.issued | 2012 | |
dc.identifier | http://hdl.handle.net/10533/241421 | |
dc.identifier | 15090007 | |
dc.identifier | WOS:000299986600006 | |
dc.identifier | no scielo | |
dc.identifier | eid=2-s2.0-83155178547 | |
dc.identifier.uri | https://repositorioslatinoamericanos.uchile.cl/handle/2250/4472760 | |
dc.description.abstract | Niemann-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.language | eng | |
dc.relation | https://doi.org/10.1016/j.bbadis.2011.11.009 | |
dc.relation | 10.1016/j.bbadis.2011.11.009 | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.rights | Atribución-NoComercial-SinDerivadas 3.0 Chile | |
dc.rights | http://creativecommons.org/licenses/by-nc-nd/3.0/cl/ | |
dc.title | Lysosomal vitamin E accumulation in Niemann-Pick type C disease. | |
dc.type | Articulo | |