An early axonopathy in a hLRRK2(R1441G) transgenic model of Parkinson disease
Mutations in the gene for LRRK2 are the most common cause of familial Parkinson's disease (PD) and patients with these mutations manifest clinical features that are indistinguishable from those of the more common sporadic form. Thus, investigations of disease mechanisms based on disease-causing LRRK...
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| Glavni autori: | , , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Elsevier
2015-10-01
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| Serija: | Neurobiology of Disease |
| Teme: | |
| Online pristup: | http://www.sciencedirect.com/science/article/pii/S0969996115300139 |
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