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Parkinson's disease: insights from pathways
Parkinson's disease (PD) typically presents in sporadic fashion, but the identification of disease-causing mutations in monogenically inherited PD genes has provided crucial insight into the pathogenesis of this disorder. Mutations in autosomal recessively inherited genes, namely parkin, PINK1...
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| Huvudupphovsmän: | , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Oxford University Press
2010
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2875048/ https://ncbi.nlm.nih.gov/pubmed/20421364 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddq167 |
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