📣 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.

Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections (2024)

First Author: Jeffries L

Attributed to: UK Infrastructure for Large-scale Clinical Genomics Research funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.gim.2023.101023

PubMed Identifier: 37947183

Publication URI: http://europepmc.org/abstract/MED/37947183

Type: Journal Article/Review

Parent Publication: Genetics in Medicine

Issue: 2

ISSN: 1098-3600