Post-translational modification and mitochondrial function in Parkinson’s disease
Parkinson’s disease (PD) is the second most common neurodegenerative disease with currently no cure. Most PD cases are sporadic, and about 5–10% of PD cases present a monogenic inheritance pattern. Mutations in more than 20 genes are associated with genetic forms of PD. Mitochondrial dysfunction is...
Furkejuvvon:
| Váldodahkkit: | , , |
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| Materiálatiipa: | Artigo |
| Giella: | Inglês |
| Almmustuhtton: |
Frontiers Media S.A.
2024-01-01
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| Ráidu: | Frontiers in Molecular Neuroscience |
| Fáttát: | |
| Liŋkkat: | https://www.frontiersin.org/articles/10.3389/fnmol.2023.1329554/full |
| Fáddágilkorat: |
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