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