Screening for TMEM230 mutations in young-onset Parkinson's disease

Dongrui Ma, Jia Nee Foo, Ebonne Yulin Ng, Yi Zhao, Jian Jun Liu, Eng King Tan*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

8 Citations (Scopus)

Abstract

TMEM230 gene mutations have been reported to be linked with Parkinson's disease (PD) recently. To investigate the prevalence of this gene in southeastern Chinese patients with PD, whole exome sequencing was performed in young-onset and familial PD patients and healthy controls in our Asian population. One heterozygous missense p.Phe121Ser mutation was detected in a healthy 76-year-old control subject and no other TMEM230 mutations were found in PD patients and controls. These data suggest that TMEM230 mutation might be a rare cause of Chinese familial and sporadic PD patients and a larger sample size will be needed to evaluate the association of TMEM230 polymorphic variants with PD.

Original languageEnglish
Pages (from-to)239.e9-239.e10
JournalNeurobiology of Aging
Volume58
DOIs
Publication statusPublished - Oct 2017
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2017 Elsevier Inc.

ASJC Scopus Subject Areas

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

Keywords

  • Mutation screening
  • Parkinson's disease
  • TMEM230
  • Whole exome sequencing

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