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“LRRK2: Autophagy and Lysosomal Activity”
It has been 15 years since the Leucine-rich repeat kinase 2 (LRRK2) gene was identified as the most common genetic cause for Parkinson’s disease (PD). The two most common mutations are the LRRK2-G2019S, located in the kinase domain, and the LRRK2-R1441C, located in the ROC-COR domain. While the LRRK...
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| Veröffentlicht in: | Front Neurosci |
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| Hauptverfasser: | , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Frontiers Media S.A.
2020
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7262160/ https://ncbi.nlm.nih.gov/pubmed/32523507 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnins.2020.00498 |
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