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NR4A2 genetic variation in sporadic Parkinson's disease: a genewide approach.
Authors:Daniel G Healy  Patrick M Abou-Sleiman  Kourosh R Ahmadi  Sonia Gandhi  Miratul M Muqit  Kailash P Bhatia  Niall P Quinn  Andrew J Lees  Janice L Holton  Tamas Revesz  Nicholas W Wood
Affiliation:Department of Molecular Neuroscience, Institute of Neurology, London, United Kingdom. d.healy@ion.ucl.ac.uk
Abstract:
The NR4A2 gene, which may cause autosomal dominant Parkinson's disease (PD), has also been reported to be a susceptibility factor for sporadic PD. Here, we use a haplotype-tagging approach in 802 PD patients and 784 controls and demonstrate that common genetic variation, including NR4A2 haplotypes, does not influence the risk of PD in the Caucasian population.
Keywords:NR4A2  Parkinson's disease  genewide study  haplotype tagging
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