ABCA7 rare variants and Alzheimer disease risk

ABCA7 rare variants and Alzheimer disease risk

Item
http://www.wikidata.org/entity/Q36982034
Late onset Alzheimer's disease genetics implicates microglial pathways in disease risk.Neuropsychiatric genomics in precision medicine: diagnostics, gene discovery, and translation.ABCA7 loss-of-function variants, expression, and neurologic disease risk.From Common to Rare Variants: The Genetic Component of Alzheimer Disease.17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression.Early-Onset Alzheimer Disease.Untangling Genetic Risk for Alzheimer's Disease.Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer's disease.ABCA7 and Pathogenic Pathways of Alzheimer's Disease.Decreased plasma β-amyloid in the Alzheimer's disease APP A673T variant carriers.An intronic VNTR affects splicing of ABCA7 and increases risk of Alzheimer's disease.Rare ABCA7 variants in 2 German families with Alzheimer disease.Whole genome sequencing of Caribbean Hispanic families with late-onset Alzheimer's disease.The Role of Genetics in Advancing Precision Medicine for Alzheimer's Disease-A Narrative Review.
P2860

ABCA7 rare variants and Alzheimer disease risk

Item
http://www.wikidata.org/entity/Q36982034
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
ABCA7 rare variants and Alzheimer disease risk
@en
type
label
ABCA7 rare variants and Alzheimer disease risk
@en
prefLabel
ABCA7 rare variants and Alzheimer disease risk
@en
P1433
P1476
P2093
P2860
P304
P31
P356
P407
P433
P478
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P577
P698
P921
P932
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P1433
P1476
ABCA7 rare variants and Alzheimer disease risk
@en
P2093
P2860
P304
P31
P356
10.1212/WNL.0000000000002627
P407
P433
P478
P50
P577
P698
P921
P932