Exon dosage analysis of parkin gene in Chinese sporadic Parkinson’s disease
Author:
Publisher
Elsevier BV
Subject
General Neuroscience
Reference17 articles.
1. A wide variety of mutations in the parkin gene are responsible for autosomal recessive Parkinsonism in Europe;Abbas;Hum. Mol. Genet.,1999
2. Parkinson’s disease dementia and potential therapeutic strategies;Caviness;CNS Neurosci. Ther.,2011
3. Familial aggregation of Parkinson’s disease: a population-based case-control study in Europe. EUROPARKINSON Study Group;Elbaz;Neurology,1999
4. Genetics of Parkinson disease: paradigm shifts and future prospects;Farrer;Nat. Rev. Genet.,2006
5. Mutation analysis of parkin, PINK1, DJ-1 and ATP13A2 genes in Chinese patients with autosomal recessive early-onset Parkinsonism;Guo;Mov. Disord.,2008
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