
A novel mutation, a C to T transition at base pair 2124 in exon 17 of the amyloid beta-protein precursor (APP) gene, has been identified by direct sequencing of amplified DNA from two Alzheimer's disease (AD) patients. A simple oligonucleotide-hybridization procedure was developed to allow population studies of this DNA variation. The mutation, which is silent at the protein level, was present in 2 out of 12 investigated AD patients, in 1 out of 60 non-AD patients and in 1 out of 30 healthy individuals. The mutation can be used as a new marker for linkage studies involving the APP gene, although more comprehensive population studies are required to determine the status of the mutation as a possible risk factor for the development of AD.
Chromosome Aberrations, Genetic Markers, Amyloid beta-Protein Precursor, Base Sequence, Genes, Alzheimer Disease, Molecular Sequence Data, Mutation, Humans, Nucleic Acid Hybridization, Codon, Polymerase Chain Reaction
Chromosome Aberrations, Genetic Markers, Amyloid beta-Protein Precursor, Base Sequence, Genes, Alzheimer Disease, Molecular Sequence Data, Mutation, Humans, Nucleic Acid Hybridization, Codon, Polymerase Chain Reaction
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