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LRRK2 Phosphorylation, More Than an Epiphenomenon
Mutations in the Leucine Rich Repeat Kinase 2 (LRRK2) gene are linked to autosomal dominant Parkinson's disease (PD), and genetic variations at the LRRK2 locus are associated with an increased risk for sporadic PD. This gene encodes a kinase that is physiologically multiphosphorylated, includin...
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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/PMC7308437/ https://ncbi.nlm.nih.gov/pubmed/32612495 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnins.2020.00527 |
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