טוען...
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: | , , , , , , , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Oxford University Press
2012
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| נושאים: | |
| גישה מקוונת: | 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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