BTB domain mutations perturbing KCTD15 oligomerisation cause a distinctive frontonasal dysplasia syndrome. (2024)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1136/jmg-2023-109531
PubMed Identifier: 38296633
Publication URI: http://europepmc.org/abstract/MED/38296633
Type: Journal Article/Review
Parent Publication: Journal of medical genetics
ISSN: 0022-2593