📣 Help Shape the Future of UKRI's Gateway to Research (GtR)

We're improving UKRI's Gateway to Research and are seeking your input! If you would be interested in being interviewed about the improvements we're making and to have your say about how we can make GtR more user-friendly, impactful, and effective for the Research and Innovation community, please email gateway@ukri.org.

Exome-wide evaluation of rare coding variants using electronic health records identifies new gene-phenotype associations (2021)

First Author: Park J

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

Parent Publication: Nature Medicine

Issue: 1

ISSN: 1078-8956