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Genetic and pharmacological evidence implicates cathepsins in Niemann-Pick C cerebellar degeneration

Niemann-Pick C1 (NPC) disease, an autosomal recessive lipid trafficking disorder caused by loss-of-function mutations in the NPC1 gene, is characterized by progressive neurodegeneration resulting in cognitive impairment, ataxia and early death. Little is known about the cellular pathways leading to...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Hum Mol Genet
Egile Nagusiak: Chung, Chan, Puthanveetil, Prasanth, Ory, Daniel S., Lieberman, Andrew P.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Oxford University Press 2016
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4787909/
https://ncbi.nlm.nih.gov/pubmed/26908626
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddw025
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