The role of mitochondria in reduced penetrance of heterozygous Parkin mutations
Parkinson´s Disease (PD) is the most common neurodegenerative movement disorder, estimated to affect up to 2% of the population over 65 years of age (Lin et al., 2019; Santos et al., 2019). Parkin (PRKN) mutations are the most common known cause of autosomal recessive early-onset PD, accounting for...
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| Format: | Doctoral Thesis |
| Language: | English |
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Università degli studi di Trento
2021
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| Online Access: | http://hdl.handle.net/11572/319705 |