Caricamento...
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...
Salvato in:
| Pubblicato in: | J Neurosci |
|---|---|
| Autori principali: | , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Society for Neuroscience
2014
|
| Soggetti: | |
| Accesso online: | 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 |
| Tags: |
Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !
|