Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. (2023)
Attributed to:
Determining the causal links and clinical significance of rare genetic variants
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1093/hmg/ddac275
PubMed Identifier: 36349687
Publication URI: http://europepmc.org/abstract/MED/36349687
Type: Journal Article/Review
Volume: 32
Parent Publication: Human molecular genetics
Issue: 8
ISSN: 0964-6906