Comprehensive analysis of<i>LRRK2</i>in publicly available Parkinson's disease cases and neurologically normal controls
Mutation of LRRK2, encoding dardarin, is the most common known genetic cause of Parkinson's disease (PD). The large size of this gene and the relative ease with which the most common mutations can be screened means that although more than 50 LRRK2 screening papers have been published, few have...
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| Main Authors: | , , , , |
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| Format: | Artigo |
| Language: | English |
| Published: |
2008
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| Online Access: | https://doi.org/10.1002/humu.20668 |
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