NR4A2 genetic variation in sporadic Parkinson's disease: A genewide approach

The NR4A2 gene, which may cause amosomal 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. (c) 2006 Movement Disorder Society