Loading...
Neurodegeneration in SCA14 is associated with increased PKCγ kinase activity, mislocalization and aggregation
Spinocerebellar ataxia type 14 (SCA14) is a subtype of the autosomal dominant cerebellar ataxias that is characterized by slowly progressive cerebellar dysfunction and neurodegeneration. SCA14 is caused by mutations in the PRKCG gene, encoding protein kinase C gamma (PKCγ). Despite the identificatio...
Saved in:
| Published in: | Acta Neuropathol Commun |
|---|---|
| Main Authors: | , , , , , , , , , |
| Format: | Artigo |
| Language: | Inglês |
| Published: |
BioMed Central
2018
|
| Subjects: | |
| Online Access: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6151931/ https://ncbi.nlm.nih.gov/pubmed/30249303 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40478-018-0600-7 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|