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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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Main Authors: Houlden, Henry, Singleton, Andrew B.
Format: Artigo
Jezik:Inglês
Izdano: 2012
Teme:
Online dostop: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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