DNAJ mutations are rare in Chinese Parkinson's disease patients and controls

Jia Nee Foo, Herty Liany, Louis C. Tan, Wing Lok Au, Kumar M. Prakash, Jianjun Liu, Eng King Tan*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

21 Citations (Scopus)

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 (<0.5%), found in healthy population controls and did not show enrichment in PD cases. Our results suggest that missense mutations in DNAJC13, DNAJC5 and DNAJC6 do not play a major role in PD in the Chinese population.

Original languageEnglish
Pages (from-to)935.e1-935.e2
JournalNeurobiology of Aging
Volume35
Issue number4
DOIs
Publication statusPublished - Apr 2014
Externally publishedYes

ASJC Scopus Subject Areas

  • General Neuroscience
  • Ageing
  • Clinical Neurology
  • Developmental Biology
  • Geriatrics and Gerontology

Keywords

  • Association
  • Chinese population
  • DNAJ family
  • Mutation
  • Parkinson's disease

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