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PMID: 1944558 Published · ppublish English Case Reports Journal Article Research Support, Non-U.S. Gov't

Early-onset Alzheimer's disease caused by mutations at codon 717 of the beta-amyloid precursor protein gene.

Nature ·Vol. 353 ·No. 6347 ·1991-10-31 ·Pages 844-6

Chartier-Harlin MC, Crawford F, Houlden H, Warren A, Hughes D, Fidani L, Goate A, Rossor M, Roques P, Hardy J

Abstract

A mutation at codon 717 of the beta-amyloid precursor protein gene has been found to cosegregate with familial Alzheimer's disease in a single family. This mutation has been reported in a further five out of approximately 100 families multiply affected by Alzheimer's disease. We have identified another family, F19, in which we have detected linkage between the beta-amyloid precursor protein gene and Alzheimer's disease. Direct sequencing of exon 17 in affected individuals from this family has revealed a base change producing a Val----Gly substitution, also at codon 717. The occurrence of a second allelic variant at codon 717 linked to the Alzheimer's phenotype supports the hypothesis that they are pathogenic mutations.

MeSH Terms
Alzheimer Disease/genetics Amino Acid Sequence Amyloid beta-Protein Precursor/genetics Base Composition Base Sequence Codon/genetics Exons Female Genes Humans Male Molecular Sequence Data Mutation Oligodeoxyribonucleotides Pedigree Polymerase Chain Reaction
Chemicals
Amyloid beta-Protein Precursor Codon Oligodeoxyribonucleotides
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Chartier-Harlin M C
Department of Biochemistry, St Mary's Hospital Medical School, Imperial College, London, UK.
Crawford F
Houlden H
Warren A
Hughes D
Fidani L
Goate A
Rossor M
Roques P
Hardy J
Article Info
Journal
Nature
Abbr.
Nature
ISSN
0028-0836
Published
1991-10-31
Pages
844-6
Language
English
Region
England
NLM ID
0410462
Subset
IM
Grants
Wellcome Trust · United Kingdom
Databases
GENBANK
S60983, X57450, X57451, X57452, X57453, X57454, X57455, X57689, X62741, X62744
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