Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome.
- Resource Type
- Article
- Authors
- Alharatani, Reham; Ververi, Athina; Beleza-Meireles, Ana; Ji, Weizhen; Mis, Emily; Patterson, Quinten T; Griffin, John N; Bhujel, Nabina; Chang, Caitlin A; Dixit, Abhijit; Konstantino, Monica; Healy, Christopher; Hannan, Sumayyah; Neo, Natsuko; Cash, Alex; Li, Dong; Bhoj, Elizabeth; Zackai, Elaine H; Cleaver, Ruth; Baralle, Diana
- Source
- Human Molecular Genetics; Jun2020, Vol. 29 Issue 11, p1900-1921, 22p
- Subject
- Language
- ISSN
- 09646906