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Leucine-Rich Repeat Kinase 2 Colocalizes with α-Synuclein in Parkinson's Disease, but Not Tau-Containing Deposits in Tauopathies
BACKGROUND: Mutations in leucine-rich repeat kinase 2 (LRRK2) are thus far the most frequent genetic cause associated with autosomal dominant and idiopathic Parkinson's disease. OBJECTIVE: To examine whether LRRK2 is directly associated with the pathological structures of Parkinson's disea...
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| Autors principals: | , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
S. Karger AG
2008
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2677749/ https://ncbi.nlm.nih.gov/pubmed/18322396 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000113708 |
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