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Genetic findings in Parkinson's disease and translation into treatment: a leading role for mitochondria?
Parkinson’s disease (PD) is a progressive neurodegenerative movement disorder and in most patients its aetiology remains unknown. Molecular genetic studies in familial forms of the disease identified key proteins involved in PD pathogenesis, and support a major role for mitochondrial dysfunction, wh...
| Autores principales: | , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
Blackwell Publishing Ltd
2008
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2268956/ https://www.ncbi.nlm.nih.gov/pubmed/17680806 http://dx.doi.org/10.1111/j.1601-183X.2007.00342.x |