Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome. (2020)
Attributed to:
GSK3 and lamellipodial dynamics in migrating neural crest cells
funded by
BBSRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1093/hmg/ddaa050
PubMed Identifier: 32196547
Publication URI: http://europepmc.org/abstract/MED/32196547
Type: Journal Article/Review
Volume: 29
Parent Publication: Human molecular genetics
Issue: 11
ISSN: 0964-6906