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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...
Enregistré dans:
| Publié dans: | Transl Neurodegener |
|---|---|
| Auteurs principaux: | , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
BioMed Central
2021
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7816312/ https://ncbi.nlm.nih.gov/pubmed/33468256 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40035-020-00229-8 |
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