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

Volume: 26

Parent Publication: Genetics in medicine : official journal of the American College of Medical Genetics

Issue: 2

ISSN: 1098-3600