Please use this identifier to cite or link to this item:
|Title:||Genetic analysis of LRRK2 A419V variant in ethnic Chinese|
|Citation:||Li, N.-N., Tan, E.-K., Chang, X.-L., Mao, X.-Y., Zhang, J.-H., Zhao, D.-M., Liao, Q., Peng, R. (2012-08). Genetic analysis of LRRK2 A419V variant in ethnic Chinese. Neurobiology of Aging 33 (8) : e1-e3. ScholarBank@NUS Repository. https://doi.org/10.1016/j.neurobiolaging.2012.02.013|
|Abstract:||Mutations in the leucine-rich repeat kinase 2 gene (. LRRK2) are the most common causes of autosomal dominant and sporadic forms of Parkinson's disease (PD). The A419V variant has been suggested to be a potential risk variant but its role among Chinese is unclear. We genotyped . LRRK2 A419V variant to investigate the association with risk of PD. A total of 1314 subjects comprising 729 patients with PD and 585 controls were genotyped. Twenty-two (3.0%) patients were heterozygous carriers for the A419V variant, and the frequency was higher compared with controls (0.7%, . p = 0.003). The association was seen among the younger age group (early onset PD patients vs. controls: . p = 0.0005), but was not significant among the older age group (late onset PD patients vs. controls: . p = 0.17). We showed a significant association of . LRRK2 A419V variant among early onset PD in the ethnic Han Chinese population but not among late onset PD. Further replication studies in additional Chinese and other Asian cohorts will be important to address its potential pathophysiologic role. © 2012 Elsevier Inc..|
|Source Title:||Neurobiology of Aging|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Nov 14, 2018
checked on Oct 26, 2018
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.