Microarray expression analysis and identification of serum biomarkers for Niemann–Pick disease, type C1

Niemann–Pick disease type C (NPC) is a lysosomal storage disorder characterized by liver disease and progressive neurodegeneration. Deficiency of either NPC1 or NPC2 leads to the accumulation of cholesterol and glycosphingolipids in late endosomes and early lysosomes. In order to identify pathologic...

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Main Authors: Cluzeau, Celine V.M., Watkins-Chow, Dawn E., Fu, Rao, Borate, Bhavesh, Yanjanin, Nicole, Dail, Michelle K., Davidson, Cristin D., Walkley, Steven U., Ory, Daniel S., Wassif, Christopher A., Pavan, William J., Porter, Forbes D.
Format: Artigo
Sprog:Inglês
Udgivet: Oxford University Press 2012
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Articles
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3406758/
https://ncbi.nlm.nih.gov/pubmed/22619379
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/dds193
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