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Gene and MicroRNA Transcriptome Analysis of Parkinson's Related LRRK2 Mouse Models
Mutations in leucine-rich repeat kinase 2 (LRRK2) are the most frequent cause of genetic Parkinson’s disease (PD). The biological function of LRRK2 and how mutations lead to disease remain poorly defined. It has been proposed that LRRK2 could function in gene transcription regulation; however, this...
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| Hauptverfasser: | , , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Public Library of Science
2014
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3888428/ https://ncbi.nlm.nih.gov/pubmed/24427314 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0085510 |
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