Exome-wide evaluation of rare coding variants using electronic health records identifies new gene-phenotype associations. (2021)
Attributed to:
UK Biobank (core renewal)
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1038/s41591-020-1133-8
PubMed Identifier: 33432171
Publication URI: http://europepmc.org/abstract/MED/33432171
Type: Journal Article/Review
Volume: 27
Parent Publication: Nature medicine
Issue: 1
ISSN: 1078-8956