Early-onset Alzheimer's disease caused by a novel mutation at codon 219 of the presenilin-1 gene

Neuroreport. 1999 Feb 25;10(3):503-7. doi: 10.1097/00001756-199902250-00011.

Abstract

Mutations in the presenilin 1 (PS1) gene are responsible for approximately 50% of early onset autosomal-dominant Alzheimer's disease cases. A PCR based mutation detection method, chemical cleavage of mismatch, was used to detect a novel PS1 mutation in the coding sequence of the PS1 gene. Sequencing confirmed a T to C transition altering a leucine to proline at codon 219 of the PS1 gene. This is a novel mutation in exon 7 of the PS1 gene occurring outside the transmembrane regions of IV and V.

Publication types

  • Case Reports

MeSH terms

  • Age of Onset
  • Aged
  • Alzheimer Disease / epidemiology*
  • Alzheimer Disease / genetics*
  • Amino Acid Substitution
  • Codon / genetics*
  • DNA / genetics
  • DNA Mutational Analysis
  • Exons / genetics
  • Female
  • Genome
  • Humans
  • Male
  • Membrane Proteins / genetics*
  • Middle Aged
  • Mutation, Missense / genetics*
  • Polymerase Chain Reaction
  • Presenilin-1

Substances

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