Role of Mendelian genes in “sporadic” Parkinson's disease
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Geriatrics and Gerontology,Neurology
Reference20 articles.
1. Parkinson's disease: from monogenic forms to genetic susceptibility factors;Lesage;Hum Mol Genet,2009
2. Translation Initiator EIF4G1 Mutations in Familial Parkinson Disease;Chartier-Harlin;Am J Hum Genet,2011
3. VPS35 mutations in Parkinson disease;Vilarino-Guell;Am J Hum Genet,2011
4. A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease;Zimprich;Am J Hum Genet,2011
5. Mutation in the alpha-synuclein gene identified in families with Parkinson's disease;Polymeropoulos;Science,1997
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