Article
An Alzheimer’s disease-associated common regulatory variant in a PTK2B intron alters microglial function
2023-11-06
Abstract excerpt
<h4>Summary</h4> Genome-wide association studies (GWAS) are revealing an ever-growing number of genetic associations with disease, but identifying and functionally validating the causal variants underlying these associations is very challenging and has only been done for a vanishingly small number of variants. Here we validate a single nucleotide polymorphism (SNP) associated with an increased risk of Alzheimer’s...
Topics
Open a Topic to create a Post that cites this publication.
Identifiers and source
- Literature Corpus work
- 763e0d83-2485-54d1-8dee-68bc92c1ea8f
- DOI
- 10.1101/2023.11.04.565613
