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The role of LRRK2 dysfunction in Parkinson’s disease
Parkinson’s disease is a common and usually sporadic neurodegenerative disorder. However, a subset of cases are inherited and, of these, mutations in the gene encoding Leucine-rich repeat kinase 2 (LRRK2) are the most frequent known genetic cause of disease. Here, we will discuss recent progress in...
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| Vydáno v: | Expert Rev Mol Med |
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| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2011
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4672634/ https://ncbi.nlm.nih.gov/pubmed/21676337 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1017/S146239941100192X |
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