| Literature DB >> 8080251 |
J Haan1, C Van Broeckhoven, C M van Duijn, E Voorhoeve, F van Harskamp, J C van Swieten, M L Maat-Schieman, R A Roos, E Bakker.
Abstract
In 31 symptomatic and 5 asymptomatic carriers of the amyloid precursor protein (APP) gene codon 693 mutation, 10 family members without mutation, and 5 carriers of the APP gene codon 692 mutation (3 with early-onset Alzheimer dementia, 2 with cerebral hemorrhage), a high frequency of the apolipoprotein E epsilon 4 allele was found. Age at onset, age at death, occurrence of dementia, and number of strokes did not differ between APP gene mutation carriers with or without epsilon 4 allele, showing that the clinical expression of these APP mutations is not influenced by the apolipoprotein E gene.Entities:
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Year: 1994 PMID: 8080251 DOI: 10.1002/ana.410360315
Source DB: PubMed Journal: Ann Neurol ISSN: 0364-5134 Impact factor: 10.422