A novel presenilin 1 mutation, I202F occurring at a previously predicted pathogenic site causing autosomal dominant Alzheimer's disease

Neurobiol Aging. 2011 Mar;32(3):556.e1-2. doi: 10.1016/j.neurobiolaging.2010.09.030. Epub 2010 Dec 7.

Abstract

We report a novel presenilin-1 (PSEN1) mutation, I202F occurring in a Welsh kindred with familial Alzheimer's disease. The average age at onset was 53 years. The I202F mutation occurs in alignment with previously reported PSEN1 mutations in the fourth transmembrane domain and confirms that PSEN1 mutations line up along transmembrane alpha-helices.

Publication types

  • Case Reports

MeSH terms

  • Alzheimer Disease / genetics
  • Alzheimer Disease / pathology
  • Female
  • Humans
  • Isoleucine / genetics*
  • Male
  • Middle Aged
  • Mutation / genetics*
  • Phenylalanine / genetics*
  • Predictive Value of Tests
  • Presenilin-1 / genetics*

Substances

  • PSEN1 protein, human
  • Presenilin-1
  • Isoleucine
  • Phenylalanine