Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice

Martin E., Enriquez A., SPARROW D., Humphreys D., McInerney-Leo A., Leo P., Duncan E., Iyer K., Greasby J., Ip E., Giannoulatou E., Sheng D., Wohler E., Dimartino C., Amiel J., Capri Y., Lehall D., Mory A., Wilnai Y., Lebenthal Y., Gharavi A., Krzemień G., Miklaszewska M., Steiner R., Raggio C., Blank R., Feldman H., Rasouly H., Sobreira N., Jobling R., Gordon C., Giampietro P., Dunwoodie S., Chapman G.

DOI

10.1093/hmg/ddaa258

Type

Journal article

Publisher

Oxford University Press (OUP)

Publication Date

2020-12-07T00:00:00+00:00

Permalink More information Close