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DJ-1 in Parkinson’s Disease: Clinical Insights and Therapeutic Perspectives
Mutations in the protein DJ-1 cause autosomal recessive forms of Parkinson’s disease (PD) and oxidized DJ-1 is found in the brains of idiopathic PD individuals. While several functions have been ascribed to DJ-1 (most notably protection from oxidative stress), its contribution to PD pathogenesis is...
Guardat en:
| Publicat a: | J Clin Med |
|---|---|
| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
MDPI
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6780414/ https://ncbi.nlm.nih.gov/pubmed/31484320 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jcm8091377 |
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