Analysis of whole genome sequence data shows association of Alzheimer’s disease with rare coding variants in ABCA7 , PSEN1 , SORL1 and TREM2

Previous studies have reported associations between risk of Alzheimer's disease (AD) or dementia and rare coding variants in a number of genes. A two-stage strategy was used in which a previously released whole exome sequenced sample was used to prioritise 100 genes showing the strongest eviden...

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Vydané v:	Journal of neurogenetics s. 1 - 10
Hlavní autori:	Curtis, David, Joseph, Shujaani
Médium:	Journal Article
Jazyk:	English
Vydavateľské údaje:	England 24.09.2025
Predmet:	ABCA7 TREM2 PSEN1 Alzheimer’s disease SORL1
ISSN:	0167-7063, 1563-5260, 1563-5260
On-line prístup:	Získať plný text
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