239
Views
23
CrossRef citations to date
0
Altmetric
Research Article

Genetic Variants in the RAB7L1 and SLC41A1 Genes of the PARK16 Locus in Chinese Parkinson's Disease Patients

, , , , , & show all
Pages 632-636 | Received 24 May 2011, Published online: 04 Aug 2011

REFERENCES

  • Chang, X. L., Mao, X. Y., Li, H. H., Zhang, J. H., Li, N. N., Burgunder, J. M., (2011). Association of GWAS loci with PD in China. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 156, 334–339.
  • Hu, Z. X., Peng, D. T., Cai, M., Pu, J. L., Lei, X. G., Yin, X. Z., (2011). A study of six point mutation analysis of LRRK2 gene in Chinese mainland patients with Parkinson's disease. Neurological Sciences.
  • Hughes, A. J., Daniel, S. E., Kilford, L. & Lees, A. J. (1992). Accuracy of clinical diagnosis of idiopathic Parkinson's disease: A clinico-pathological study of 100 cases. Journal of Neurology, Neurosurgery & Psychiatry, 55, 181–184.
  • Mata, I. F., Yearout, D., Alvarez, V., Coto, E., de Mena, L., Ribacoba, R., (2011 April). Replication of MAPT and SNCA, but not PARK16-18, as susceptibility genes for parkinson's disease. Movement Disorders, 26(5), 819–823.
  • Ramirez, A., Ziegler, A., Winkler, S., Kottwitz, J., Giesen, R., Díaz-Grez, F., (2011). Association of Parkinson disease to PARK16 in a Chilean sample. Parkinsonism & Related Disorders, 17(1), 70–71.
  • Samii, A., Nutt, J. G. & Ransom, B. R. (2004). Parkinson's disease. Lancet, 363, 1783–1793.
  • Satake, W., Nakabayashi, Y., Mizuta, I., Hirota, Y., Ito, C., Kubo, M., Kawaguchi, T., (2009). Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. Nature Genetics, 41, 1303–1307.
  • Tan, E. K., Kwok, H. H., Tan, L. C., Zhao, W. T., Prakash, K. M., Au, W. L., (2010). Analysis of GWAS-linked loci in Parkinson disease reaffirms PARK16 as a susceptibility locus. Neurology, 75, 508–512.
  • The UK Parkinson's Disease Consortium and The Wellcome Trust Case Control Consortium 2. (2011). Dissection of the genetics of Parkinson's disease identifies an additional association 5′ of SNCA and multiple associated haplotypes at 17q21. Human Molecular Genetics, 20(2), 345–353.
  • Tucci, A., Nalls, M. A., Houlden, H., Revesz, T., Singleton, A. B., Wood, N. W., (2010). Genetic variability at the PARK16 locus. European Journal of Human Genetics, 18, 1356–1359.
  • Vilariño-Güell, C., Ross, O. A., Aasly, J. O., White, L. R., Rajput, A., Rajput, A. H., (2010). An independent replication of PARK16 in Asian samples. Neurology, 75, 2248–2249.
  • Wiśniewski, J. R., Zougman, A., Krüger, S., Ziókowski, P., Pudeko, M., Bebenek, M., (2008). Constitutive and dynamic phosphorylation and acetylation sites on NUCKS, a hypermodified nuclear protein, studied by quantitative proteomics. Proteins, 73, 710–718.
  • Xiromerisiou, G., Dardiotis, E., Tsimourtou, V., Kountra, P. M., Paterakis, K. N., Kapsalaki, E. Z., (2010). Genetic basis of Parkinson disease. Neurosurgical Focus, 28, E7.
  • Zhang, B. R., Hu, Z. X., Yin, X. Z., Cai, M., Zhao, G. H., Liu, Z. R., (2010). Mutation analysis of parkin and PINK1 genes in early-onset Parkinson's disease in China. Neuroscience Letters, 477, 19–22.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.