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Lysosome and endoplasmic reticulum quality control pathways in Niemann-Pick type C disease

Lysosomal storage diseases result from inherited deficiencies of lysosomal hydrolytic activities or lipid transport. Collectively, these disorders are a common cause of morbidity in the pediatric population and are often associated with severe neurodegeneration. Among this group of diseases is Niema...

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Podrobná bibliografie
Vydáno v:Brain Res
Hlavní autoři: Schultz, Mark L., Krus, Kelsey L., Lieberman, Andrew P.
Médium: Artigo
Jazyk:Inglês
Vydáno: 2016
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5542880/
https://ncbi.nlm.nih.gov/pubmed/27026653
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.brainres.2016.03.035
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