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Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome (2020)

First Author: Alharatani R

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

Parent Publication: Human Molecular Genetics

Issue: 11

ISSN: 0964-6906