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Parkinson’s Disease-Associated Pathogenic VPS35 Mutation Causes Complex I Deficits
Defect in the complex I of the mitochondrial electron-transport chain is a characteristic of Parkinson’s disease (PD) which is thought to play a critical role in the disease pathogenesis. Mutations in vacuolar sorting protein 35 (VPS35) cause autosomal dominant PD and we recently demonstrated that p...
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| Publicado no: | Biochim Biophys Acta |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5659972/ https://ncbi.nlm.nih.gov/pubmed/28765075 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bbadis.2017.07.032 |
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