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Models of LRRK2 associated Parkinson’s disease
Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene are the most common genetic causes of Parkinson’s disease (PD), and also one of the strongest genetic risk factors in sporadic PD. The LRRK2 protein contains a GTPase domain and a kinase domain, and several protein-protein interaction domain...
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| I publikationen: | Adv Neurobiol |
|---|---|
| Huvudupphovsmän: | , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
2017
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5535810/ https://ncbi.nlm.nih.gov/pubmed/28353284 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/978-3-319-49969-7_9 |
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