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Function and dysfunction of leucine-rich repeat kinase 2 (LRRK2): Parkinson’s disease and beyond
Mutations in leucine-rich repeat kinase 2 (LRRK2) are the most common cause of familial Parkinson’s disease (PD). As such, functions and dysfunctions of LRRK2 in PD have been the subject of extensive investigation. In addition to PD, increasing evidence is suggesting that LRRK2 is associated with a...
Sparad:
| I publikationen: | BMB Rep |
|---|---|
| Huvudupphovsmän: | , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Korean Society for Biochemistry and Molecular
Biology
2015
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4578562/ https://ncbi.nlm.nih.gov/pubmed/25703537 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5483/BMBRep.2015.48.5.032 |
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