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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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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:J Neurosci
Egile Nagusiak: Tsunemi, Taiji, Hamada, Kana, Krainc, Dimitri
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Society for Neuroscience 2014
Gaiak:
Sarrera elektronikoa: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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