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

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Keywords: Alzheimer disease; Val717Phe mutation; amyloid precursor protein; hereditary; phenotype

Document Type: Research Article

Affiliations: 1: Departments of Neurology 2: Department of Psychiatry, Kálmán Pándy County Hospital, Gyula 3: Medical Genetics, Albert Szent-Györgyi Clinical Center, Faculty of Medicine, University of Szeged 4: Institute of Genomic Medicine and Rare Disorders, Semmelweis University, Budapest, Hungary 5: Departments of Neurology, MTA-SZTE Neuroscience Research Group, University of Szeged, Szeged

Publication date: October 1, 2017

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