Niemann-Pick disease type C1 is a sphingosine storage disease that causes deregulation of lysosomal calcium.
dc.contributor.author | Lloyd-Evans, E. | |
dc.contributor.author | Morgan, A. J. | |
dc.contributor.author | He, X. | |
dc.contributor.author | Smith, D. A. | |
dc.contributor.author | Elliot-Smith, E. | |
dc.contributor.author | Sillence, Daniel J. | |
dc.contributor.author | Churchill, G. C. | |
dc.contributor.author | Schuchman, E. H. | |
dc.contributor.author | Galione, A. | |
dc.contributor.author | Platt, Frances M. | |
dc.date.accessioned | 2009-11-17T11:55:00Z | |
dc.date.available | 2009-11-17T11:55:00Z | |
dc.date.issued | 2008-10-26 | |
dc.identifier.citation | Lloyd-Evans, E. et al. (2008) Niemann-Pick disease type C1 is a sphingosine storage disease that causes deregulation of lysosomal calcium. Nature Medicine, 14 (11), pp. 1247-1255. | en |
dc.identifier.doi | https://doi.org/10.1038/nm.1876 | |
dc.identifier.issn | 1546-170X | |
dc.identifier.issn | 1078-8956 | |
dc.identifier.uri | http://hdl.handle.net/2086/2864 | |
dc.language.iso | en | en |
dc.peerreviewed | Yes | en |
dc.publisher | Nature Publishing Group | en |
dc.ref2014.selected | 1365591152_9411495636644_3_1 | |
dc.researchgroup | Pharmacology | |
dc.researchinstitute | Leicester Institute for Pharmaceutical Innovation - From Molecules to Practice (LIPI) | en |
dc.title | Niemann-Pick disease type C1 is a sphingosine storage disease that causes deregulation of lysosomal calcium. | en |
dc.type | Article | en |
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