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
Volume31
Issue number4
DOIs
Publication statusPublished - Jan 1 2017

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Amyloid beta-Protein Precursor
Alzheimer Disease
Phenotype
Mutation
Genes

Keywords

  • 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

The Report of p.Val717Phe Mutation in the APP Gene in a Hungarian Family with Alzheimer Disease : A Phenomenological Study. / Zádori, Dénes; Füvesi, Judit; Timár, Erzsébet; Horváth, Emese; Bencsik, Renáta; Szépfalusi, Noémi; Must, Anita; Vécsei, L.; Molnár, Mária Judit; Klivényi, P.

In: Alzheimer Disease and Associated Disorders, Vol. 31, No. 4, 01.01.2017, p. 343-345.

Research output: Contribution to journalArticle

Zádori, Dénes ; Füvesi, Judit ; Timár, Erzsébet ; Horváth, Emese ; Bencsik, Renáta ; Szépfalusi, Noémi ; Must, Anita ; Vécsei, L. ; Molnár, Mária Judit ; Klivényi, P. / The Report of p.Val717Phe Mutation in the APP Gene in a Hungarian Family with Alzheimer Disease : A Phenomenological Study. In: Alzheimer Disease and Associated Disorders. 2017 ; Vol. 31, No. 4. pp. 343-345.
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