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The genetics of Parkinson’s disease: progress and therapeutic implications
The past 15 years has witnessed tremendous progress in our understanding of the genetic basis for Parkinson’s disease (PD). Notably, while most mutations, such as those in SNCA, PINK1, PARK2, PARK7, PLA2G6, FBXO7, and ATP13A2, are a rare cause of disease, one particular mutation in LRRK2, has been f...
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| Main Authors: | , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
2013
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3578399/ https://ncbi.nlm.nih.gov/pubmed/23389780 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mds.25249 |
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