A DNA repair disorder caused by de novo monoallelic DDB1 variants is associated with a neurodevelopmental syndrome. (2021)
Attributed to:
Developing diagnostic methods for clinical genetics - phenotyping from faces in photos.
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2021.03.007
PubMed Identifier: 33743206
Publication URI: http://europepmc.org/abstract/MED/33743206
Type: Journal Article/Review
Volume: 108
Parent Publication: American journal of human genetics
Issue: 4
ISSN: 0002-9297