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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...
Gorde:
| Argitaratua izan da: | Transl Neurodegener |
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| Egile Nagusiak: | , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
BioMed Central
2021
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| Gaiak: | |
| Sarrera elektronikoa: | 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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