A systematic review of familial Alzheimer's disease: Differences in presentation of clinical features among three mutated genes and potential ethnic differences
Open Access
- 1 February 2016
- journal article
- review article
- Published by Elsevier BV in Journal of the Formosan Medical Association
- Vol. 115 (2), 67-75
- https://doi.org/10.1016/j.jfma.2015.08.004
Abstract
No abstract availableKeywords
This publication has 90 references indexed in Scilit:
- Symptom onset in autosomal dominant Alzheimer diseaseNeurology, 2014
- Familial Alzheimer's disease sustained by presenilin 2 mutations: Systematic review of literature and genotype–phenotype correlationNeuroscience & Biobehavioral Reviews, 2014
- Locus‐specific mutation databases for neurodegenerative brain diseasesHuman Mutation, 2012
- Early-Onset Familial Alzheimer's Disease (EOFAD)Canadian Journal of Neurological Sciences, 2012
- Genetic screening of Alzheimer's disease genes in Iberian and African samples yields novel mutations in presenilins and APPNeurobiology of Aging, 2010
- Alzheimer’s disease phenotypes and genotypes associated with mutations in presenilin 2Brain, 2010
- 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
- Amyloid precursor protein gene mutation in early-onset Alzheimer's diseaseThe Lancet, 1991
- Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's diseaseNature, 1991