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LRRK2 in Parkinson's disease – drawing the curtain of penetrance: a commentary
Parkinson's disease is the most common neurodegenerative movement disorder and affects about 2% of the population over the age of 60 years. In 2004, mutations in the LRRK2 gene were first described and turned out to be the most frequent genetic cause of familial and sporadic Parkinson's di...
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| Formato: | Texto |
| Lenguaje: | English |
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BioMed Central
2008
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2607298/ https://www.ncbi.nlm.nih.gov/pubmed/18986509 http://dx.doi.org/10.1186/1741-7015-6-33 |