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LRRK2 links genetic and sporadic Parkinson’s disease
The past two decades in research has revealed the importance of leucine-rich repeat kinase 2 (LRRK2) in both monogenic and sporadic forms of Parkinson’s disease (PD). In families, mutations in LRRK2 can cause PD with age-dependent but variable penetrance and genome-wide association studies have foun...
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| Veröffentlicht in: | Biochem Soc Trans |
|---|---|
| Hauptverfasser: | , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2019
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6563926/ https://ncbi.nlm.nih.gov/pubmed/30837320 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BST20180462 |
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