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The A53E α-Synuclein Pathological Mutation Demonstrates Reduced Aggregation Propensity in vitro and in Cell Culture
Mutations in the gene that encodes α-synuclein (αS) are a known cause of Parkinson's disease. αS is also the major component of pathological inclusions that characterize this disorder and a spectrum of other neurodegenerative diseases termed synucleinopathies. The effects of the most recently i...
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| Publicado no: | Neurosci Lett |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4476064/ https://ncbi.nlm.nih.gov/pubmed/25892596 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neulet.2015.04.022 |
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