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Molecular Mechanisms of α-Synuclein and GBA1 in Parkinson’s Disease
Parkinson’s disease (PD) is a neurodegenerative movement disorder characterized pathologically by the presence of Lewy bodies comprised of insoluble alpha-synuclein. Pathological, clinical and genetic studies demonstrate that mutations in the GBA1 gene, which encodes the lysosomal enzyme glucocerebr...
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| Publicat a: | Cell Tissue Res |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5916529/ https://ncbi.nlm.nih.gov/pubmed/29064079 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00441-017-2704-y |
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