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Differential response of the liver to bile acid treatment in a mouse model of Niemann-Pick disease type C
Niemann-Pick disease type C (NPC) disease is a neurodegenerative lysosomal storage disease caused by mutations in the NPC1 or NPC2 genes. Liver disease is also a common feature of NPC that can present as cholestatic jaundice in the neonatal period. Liver enzymes can remain elevated above the normal...
में बचाया:
| में प्रकाशित: | Wellcome Open Res |
|---|---|
| मुख्य लेखकों: | , , , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
F1000 Research Limited
2018
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5639931/ https://ncbi.nlm.nih.gov/pubmed/29062912 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12688/wellcomeopenres.12431.2 |
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