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Leucine-rich repeat kinase 2 mutations and Parkinson’s disease: three questions
Mutations in the gene encoding LRRK2 (leucine-rich repeat kinase 2) were first identified in 2004 and have since been shown to be the single most common cause of inherited Parkinson’s disease. The protein is a large GTP-regulated serine/threonine kinase that additionally contains several protein–pro...
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| Hoofdauteurs: | , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
American Society for Neurochemistry
2009
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2695577/ https://ncbi.nlm.nih.gov/pubmed/19570025 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/AN20090007 |
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