Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice.
- Resource Type
- Article
- Authors
- Martin, Ella M M A; Enriquez, Annabelle; Sparrow, Duncan B; Humphreys, David T; McInerney-Leo, Aideen M; Leo, Paul J; Duncan, Emma L; Iyer, Kavitha R; Greasby, Joelene A; Ip, Eddie; Giannoulatou, Eleni; Sheng, Delicia; Wohler, Elizabeth; Dimartino, Clémantine; Amiel, Jeanne; Capri, Yline; Lehalle, Daphné; Mory, Adi; Wilnai, Yael; Lebenthal, Yael
- Source
- Human Molecular Genetics; Nov2020, Vol. 29 Issue 22, p3662-3678, 17p
- Subject
- Language
- ISSN
- 09646906