Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.neurobiolaging.2013.09.018
Title: DNAJ mutations are rare in Chinese Parkinson's disease patients and controls
Authors: Foo, J.N.
Liany, H.
Tan, L.C.
Au, W.-L.
Prakash, K.-M.
Liu, J.
Tan, E.-K. 
Keywords: Association
Chinese population
DNAJ family
Mutation
Parkinson's disease
Issue Date: Apr-2014
Source: Foo, J.N., Liany, H., Tan, L.C., Au, W.-L., Prakash, K.-M., Liu, J., Tan, E.-K. (2014-04). DNAJ mutations are rare in Chinese Parkinson's disease patients and controls. Neurobiology of Aging 35 (4) : 935.e1-935.e2. ScholarBank@NUS Repository. https://doi.org/10.1016/j.neurobiolaging.2013.09.018
Abstract: Mutations in DNAJC13, DNAJC6 and DNAJC5 have been implicated in Parkinson's disease (PD). To determine if rare coding variants in these genes play a role in PD risk in the Chinese population, we sequenced all coding exons of the three genes in 99 early-onset PD cases and 99 controls, and genotyped 8 missense variants in another 711 PD cases and 539 controls. Besides two common missense variants that did not show association with PD, the remaining missense variants were extremely rare (
Source Title: Neurobiology of Aging
URI: http://scholarbank.nus.edu.sg/handle/10635/110029
ISSN: 01974580
DOI: 10.1016/j.neurobiolaging.2013.09.018
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