Genetic analysis of ATP10B for Parkinson's disease in Japan

Parkinsonism Relat Disord. 2021 Jul:88:10-12. doi: 10.1016/j.parkreldis.2021.05.020. Epub 2021 May 29.

Abstract

Compound heterozygosity of ATP10B is thought to be a risk factor for young-onset Parkinson's disease (PD). We genetically screened 245 patients with young-onset sporadic PD and 33 patients with autosomal recessive PD for ATP10B. All 13 identified gene variants were heterozygous with little evidence of the pathogenicity.

Keywords: ATP10B; Familial Parkinson's disease; Gene variants.

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphatases / genetics*
  • Adult
  • Age of Onset
  • Aged
  • Female
  • Genetic Predisposition to Disease / epidemiology
  • Genetic Predisposition to Disease / genetics
  • Genetic Testing
  • Humans
  • Japan / epidemiology
  • Male
  • Membrane Transport Proteins / genetics*
  • Middle Aged
  • Parkinson Disease / epidemiology
  • Parkinson Disease / genetics*
  • Risk Factors

Substances

  • Membrane Transport Proteins
  • Adenosine Triphosphatases