📣 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.

Disease-specific variant pathogenicity prediction significantly improves variant interpretation in inherited cardiac conditions (2021)

First Author: Zhang X
Attributed to:  The Alan Turing Institute funded by EPSRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41436-020-00972-3

PubMed Identifier: 33046849

Publication URI: http://europepmc.org/abstract/MED/33046849

Type: Journal Article/Review

Parent Publication: Genetics in Medicine

Issue: 1

ISSN: 1098-3600