Novel presenilin-1 Y159F sequence variant associated with early-onset Alzheimer's disease NEUROSCIENCE LETTERS Kerchner, G. A., Holbrook, K. 2012; 531 (2): 142-144


Mutations in the gene for presenilin-1 cause familial, early-onset Alzheimer's disease.We report the case of a 43-year-old woman presenting with progressive cognitive decline and a family history of early-onset dementia. Her workup included cerebrospinal fluid amyloid-beta, tau, and phospho-tau levels, as well as genetic sequencing of genes implicated in familial Alzheimer's disease.Cerebrospinal fluid biomarkers were consistent with a diagnosis of Alzheimer's disease. A novel nucleotide sequence variant (A476T) was discovered in one allele for presenilin-1, corresponding to a missense tyrosine-to-phenylalanine change at codon 159 (Y159F). An affected maternal uncle carried the same allele. The sequence variant occurs in a conserved region of the gene near other previously reported mutations.This novel presenilin-1 sequence variant cosegregated with early onset dementia in the proband and at least one other affected family member, and likely represents a mutation causing familial, early-onset Alzheimer's disease.

View details for DOI 10.1016/j.neulet.2012.10.037

View details for Web of Science ID 000312612800016

View details for PubMedID 23123781