Loss of Parkin impairs mitochondrial function and leads to muscle atrophy
Parkinson's disease is a neurodegenerative disease characterized by tremors, muscle stiffness, and muscle weakness. Molecular genetic analysis has confirmed that mutations in PARKIN and PINK1 genes, which play major roles in mitochondrial quality control and mitophagy, are frequently associated...
| Hlavní autoři: | , , , , |
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| Další autoři: | |
| Médium: | Journal Article |
| Jazyk: | English |
| Vydáno: |
2020
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| Témata: | |
| On-line přístup: | https://hdl.handle.net/10356/138111 |