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2003 | 44 | 2 | 231-234

Article title

Molecular genetics of Alzheimer?s disease: Presenilin 1 gene analysis in a cohort of patients from the Pozna? region

Title variants

Languages of publication

EN

Abstracts

EN
Alzheimer?s disease (AD) is a progressive neurodegenerative disorder characterized by memory loss and personality changes. Pathological hallmarks of AD are: deposition of amyloid plaques and neurofibrillary tangles in the brain, accompanied by neuronal and synaptic loss. The genetic background of AD is heterogeneous and strongly depends on the form of the disease. In most of the families with early-onset AD (EOAD) (10% of the total population of patients), the disease segregates as an autosomal dominant fully penetrant trait. To date, some missense mutations in three genes encoding the amyloid precursor protein, presenilin 1 (PS1) and 2 (PS2) have been found to cause familial EOAD. We screened for mutations in the presenilin genes in a sample of 55 patients with familial or sporadic form of EOAD from the Poznan region. We found 4 missense mutations in the PS1 gene: A246E in exon 7, P267L in exon 8, E318G in exon 9, and L424R in exon 12 among 5 unrelated patients. The frequency of PS1 mutations was 11% (5 of 55) in the whole sample of the patients with EOAD or 50% (3 of 6) if the analysis was restricted to familial cases with a positive history of dementia in the patient?s family.

Discipline

Year

Volume

44

Issue

2

Pages

231-234

Physical description

Contributors

author
author
author
author
author
author

References

Document Type

SHORT COMMUNICA

Publication order reference

A. Kowalska, Institute of Human Genetics, Polish Academy of Sciences, ul. Strzeszynska 32, 60-479 Poznan, Poland

Identifiers

YADDA identifier

bwmeta1.element.element-from-psjc-b9be5fd3-bf43-39b7-be8f-3b7021fa3c85
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