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Multitasking guardian of mitochondrial quality: Parkin function and Parkinson’s disease
The familial form of Parkinson’s disease (PD) is linked to mutations in specific genes. The mutations in parkin are one of the most common causes of early-onset PD. Mitochondrial dysfunction is an emerging active player in the pathology of neurodegenerative diseases, because mitochondria are highly...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7816312/ https://www.ncbi.nlm.nih.gov/pubmed/33468256 http://dx.doi.org/10.1186/s40035-020-00229-8 |