PSEN1 variants in Korean patients with clinically suspicious early-onset familial Alzheimer’s disease
Published 2020 View Full Article
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Title
PSEN1 variants in Korean patients with clinically suspicious early-onset familial Alzheimer’s disease
Authors
Keywords
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Journal
Scientific Reports
Volume 10, Issue 1, Pages -
Publisher
Springer Science and Business Media LLC
Online
2020-02-26
DOI
10.1038/s41598-020-59829-z
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Note: Only part of the references are listed.- A novel mutation in PSEN1 (p.T119I) in an Argentine family with early- and late-onset Alzheimer's disease
- (2019) Tatiana Itzcovich et al. NEUROBIOLOGY OF AGING
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- Presenilin-1 Mutations in Alzheimer's Disease: An Update on Genotype-Phenotype Relationships
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- Clinical-Genetic Correlations in Familial Alzheimer's Disease Caused by Presenilin 1 Mutations
- (2017) Estrella Gómez-Tortosa et al. JOURNAL OF ALZHEIMERS DISEASE
- Clinical phenotype and genetic associations in autosomal dominant familial Alzheimer’s disease: a case series
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- (2012) Marc Cruts et al. HUMAN MUTATION
- Novel presenilin-1 Y159F sequence variant associated with early-onset Alzheimer's disease
- (2012) Geoffrey A. Kerchner et al. NEUROSCIENCE LETTERS
- The diagnosis of dementia due to Alzheimer’s disease: Recommendations from the National Institute on Aging-Alzheimer’s Association workgroups on diagnostic guidelines for Alzheimer's disease
- (2011) Guy M. McKhann et al. Alzheimers & Dementia
- Review Article: Genetics of Alzheimer Disease
- (2010) Lynn M. Bekris et al. JOURNAL OF GERIATRIC PSYCHIATRY AND NEUROLOGY
- Seoul Neuropsychological Screening Battery-Dementia Version (SNSB-D): A Useful Tool for Assessing and Monitoring Cognitive Impairments in Dementia Patients
- (2010) Hyun-Jung Ahn et al. JOURNAL OF KOREAN MEDICAL SCIENCE
- Genetic testing in familial AD and FTD: Mutation and phenotype spectrum in a Danish cohort
- (2009) SG Lindquist et al. CLINICAL GENETICS
- A novel presenilin 1 mutation (L282F) in familial Alzheimer’s disease
- (2009) Tsuyoshi Hamaguchi et al. JOURNAL OF NEUROLOGY
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