Early-onset Alzheimer's disease with a presenilin-1 mutation at the site corresponding to the Volga German presenilin-2 mutation

Ann Neurol. 1997 Jul;42(1):124-8. doi: 10.1002/ana.410420121.

Abstract

We describe a new mutation causing Alzheimer's disease (AD) in presenilin-1 (N135D) that is at the homologous site to the presenilin 2 mutation (N141I) in Volga German kindreds. The phenotype of PS1 N135D is an early-onset (34-38 years) disease. The mutation forms part of, and extends, the alpha-helical array of mutations in transmembrane 2 of the presenilins and leads to the suggestion that disruption of this helical face is the molecular insult that leads to disease.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Alzheimer Disease / genetics*
  • Female
  • Humans
  • Male
  • Membrane Proteins / genetics*
  • Models, Genetic
  • Mutation*
  • Pedigree
  • Phenotype
  • Presenilin-1
  • Sequence Homology

Substances

  • Membrane Proteins
  • PSEN1 protein, human
  • Presenilin-1