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

Alzheimer disease and associated disorders - 1 Jan 2000

Zádori Dénes, Füvesi Judit, Timár Erzsébet, Horváth Emese, Bencsik Renáta, Szépfalusi Noémi, Must Anita, Vécsei László, Molnár Mária Judit, Klivényi Péter

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Identifiers

PMID: 28796010
DOI: 10.1097/WAD.0000000000000206

Genes

APP

Variants

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Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

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The Report of p.Val717Phe Mutation in the APP Gene in a Hungarian Family With Alzheimer Disease: A Phenomenological Study.PMID 28796010Read ↗

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The Uppsala APP deletion causes early onset autosomal dominant Alzheimer’s disease by altering APP processing and increasing amyloid β fibril formationSemantic proximity Read ↗

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