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ATP13A2/PARK9 Regulates Secretion of Exosomes and α-Synuclein
Kufor–Rakeb syndrome (KRS) is caused by loss-of-function mutations in ATP13A2 (PARK9) and characterized by juvenile-onset parkinsonism, pyramidal signs, and cognitive decline. Previous studies suggested that PARK9 deficiency causes lysosomal dysfunction and α-synuclein (α-syn) accumulation, whereas...
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| Vydáno v: | J Neurosci |
|---|---|
| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Society for Neuroscience
2014
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4228131/ https://ncbi.nlm.nih.gov/pubmed/25392495 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.1629-14.2014 |
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