📣 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.

A method for analyzing multiple continuous phenotypes in rare variant association studies allowing for flexible correlations in variant effects. (2016)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/ejhg.2016.8

PubMed Identifier: 26860061

Publication URI: http://europepmc.org/abstract/MED/26860061

Type: Journal Article/Review

Volume: 24

Parent Publication: European journal of human genetics : EJHG

Issue: 9

ISSN: 1018-4813