Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease
Published 2015 View Full Article
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Title
Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease
Authors
Keywords
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Journal
NATURE GENETICS
Volume 47, Issue 5, Pages 445-447
Publisher
Springer Nature
Online
2015-03-25
DOI
10.1038/ng.3246
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- (2012) M. Allen et al. NEUROLOGY
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- 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
- Rare-Variant Association Testing for Sequencing Data with the Sequence Kernel Association Test
- (2011) Michael C. Wu et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor
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- (2008) Augustine Kong et al. NATURE GENETICS
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