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LRRK2 in Parkinson's disease and dementia with Lewy bodies
BACKGROUND: Mutations in LRRK2 encoding leucine-rich repeat kinase 2 are thus far the most frequent genetic cause associated with autosomal dominant and idiopathic Parkinson's disease (PD). To examine whether LRRK2 is directly associated with neuropathology of PD and other related disorders, we...
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| Asıl Yazarlar: | , , , , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BioMed Central
2006
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1693553/ https://ncbi.nlm.nih.gov/pubmed/17137507 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1326-1-17 |
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