Homozygosity of the autosomal dominant Alzheimer disease presenilin 1 E280A mutation

Neurology. 2015 Jan 13;84(2):206-8. doi: 10.1212/WNL.0000000000001130. Epub 2014 Dec 3.
No abstract available

MeSH terms

  • Adult
  • Alzheimer Disease / genetics*
  • Child
  • Colombia
  • Female
  • Homozygote*
  • Humans
  • Male
  • Middle Aged
  • Mutation*
  • Presenilin-1 / genetics*

Substances

  • PSEN1 protein, human
  • Presenilin-1

Supplementary concepts

  • Alzheimer disease, familial, type 3