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Exploring the Impact of PARK2 Mutations on the Total and Mitochondrial Proteome of Human Skin Fibroblasts
Mutations in PARK2 gene are the most frequent cause of familial forms of Parkinson’s disease (PD). This gene encodes Parkin, an E3 ubiquitin ligase involved in several cellular mechanisms, including mitophagy. Parkin loss-of-function is responsible for the cellular accumulation of damaged mitochondr...
Autores principales: | Zilocchi, Mara, Colugnat, Ilaria, Lualdi, Marta, Meduri, Monica, Marini, Federica, Corasolla Carregari, Victor, Moutaoufik, Mohamed Taha, Phanse, Sadhna, Pieroni, Luisa, Babu, Mohan, Garavaglia, Barbara, Fasano, Mauro, Alberio, Tiziana |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7300190/ https://www.ncbi.nlm.nih.gov/pubmed/32596240 http://dx.doi.org/10.3389/fcell.2020.00423 |
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