Fine-mapping across diverse ancestries drives the discovery of putative causal variants underlying human complex traits and diseases. (2023)
Attributed to:
UK Biobank (core renewal)
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1101/2023.01.07.23284293
PubMed Identifier: 36711496
Publication URI: http://europepmc.org/abstract/MED/36711496
Type: Journal Article/Review
Parent Publication: medRxiv : the preprint server for health sciences