Screening of the mis-sense mutation producing the 717Val → Ile substitution in the amyloid precursor protein in Japanese familial and sporadic Alzheimer's disease
- 1 July 1993
- journal article
- Published by Elsevier in Journal of the Neurological Sciences
- Vol. 117 (1-2) , 12-15
- https://doi.org/10.1016/0022-510x(93)90147-q
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- A mutation in the Amyloid Precursor Protein Associated with Hereditary Alzheimer's DiseaseScience, 1991
- Early-onset Alzheimer's disease caused by mutations at codon 717 of the β-amyloid precursor protein geneNature, 1991
- Screening for the β-amyloid precursor protein mutation (APP717: Val → Ile) in extended pedigrees with early onset Alzheimer's diseaseNeuroscience Letters, 1991
- Amyloid precursor protein gene mutation in early-onset Alzheimer's diseaseThe Lancet, 1991
- Mis-sense mutation Val→Ile in exon 17 of amyloid precursor protein gene in Japanese familial Alzheimer's diseaseThe Lancet, 1991
- Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's diseaseNature, 1991
- Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorderNature, 1990
- Genomic organization of the human amyloid beta-protein precursor geneGene, 1990
- The PreA4695precursor protein of Alzheimer's disease A4 amyloid is encoded by 16 exonsNucleic Acids Research, 1989
- Clinical diagnosis of Alzheimer's diseaseNeurology, 1984