The role of monogenic genes in idiopathic Parkinson’s disease
In the past two decades, mutations in multiple genes have been linked to autosomal dominant or recessive forms of monogenic Parkinson’s disease (PD). Collectively, these monogenic (often familial) cases account for less than 5% of all PD, the majority being apparently sporadic cases. More recently,...
| Hlavní autoři: | , , , |
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| Médium: | Článek |
| Jazyk: | English |
| Vydáno: |
Elsevier
2019-04-01
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| Edice: | Neurobiology of Disease |
| Témata: | |
| On-line přístup: | http://www.sciencedirect.com/science/article/pii/S0969996118306685 |