Very early-onset familial Alzheimer's disease: a novel presenilin 1 mutation
Author:
Publisher
Wiley
Subject
Psychiatry and Mental health,Geriatrics and Gerontology
Reference11 articles.
1. Molecular genetics of Alzheimer's disease
2. Presymptomatic cognitive deficits in individuals at risk of familial Alzheimer's disease. A longitudinal prospective study
3. Environmental risk factors for Alzheimer's disease: their relationship to age of onset and to familial or sporadic types
4. Monogenic determinants of familial Alzheimer's disease: presenilin-1 mutations
5. Utility of the Apolipoprotein E Genotype in the Diagnosis of Alzheimer's Disease
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1. Mixed Pathologies in a Subject with a Novel PSEN1 G206R Mutation;Journal of Alzheimer's Disease;2022-12-06
2. Early‐Onset Dementia‐Parkinsonism with Rapid Development of Motor Fluctuations and Dyskinesia Due to PSEN1 G206V Pathogenic Variant;Movement Disorders Clinical Practice;2022-11-22
3. Genetics, Functions, and Clinical Impact of Presenilin-1 (PSEN1) Gene;International Journal of Molecular Sciences;2022-09-19
4. Gene mutations associated with early onset familial Alzheimer’s disease in China: An overview and current status;Molecular Genetics & Genomic Medicine;2020-08-06
5. Novel presenilin 1 and 2 double knock-out cell line for in vitro validation of PSEN1 and PSEN2 mutations;Neurobiology of Disease;2020-05
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