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The genetics and neuropathology of Parkinson’s disease
There has been tremendous progress toward understanding the genetic basis of Parkinson’s disease and related movement disorders. We summarize the genetic, clinical and pathological findings of autosomal dominant disease linked to mutations in SNCA, LRRK2, ATXN2, ATXN3, MAPT, GCH1, DCTN1 and VPS35. W...
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| Hlavní autoři: | , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2012
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3589971/ https://ncbi.nlm.nih.gov/pubmed/22806825 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00401-012-1013-5 |
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