The Report of p.Val717Phe Mutation in the APP Gene in a Hungarian Family with Alzheimer Disease: A Phenomenological Study

Dénes Zádori, Judit Füvesi, Erzsébet Timár, Emese Horváth, Renáta Bencsik, Noémi Szépfalusi, Anita Must, L. Vécsei, Mária Judit Molnár, P. Klivényi

Research output: Contribution to journalArticle

Original languageEnglish
Pages (from-to)343-345
Number of pages3
JournalAlzheimer Disease and Associated Disorders
Issue number4
Publication statusPublished - Jan 1 2017


  • Alzheimer disease
  • amyloid precursor protein
  • hereditary
  • phenotype
  • Val717Phe mutation

ASJC Scopus subject areas

  • Clinical Psychology
  • Gerontology
  • Geriatrics and Gerontology
  • Psychiatry and Mental health

Cite this