학술논문
Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice
Document Type
Article
Author
Martin, E.M.M.A.; Enriquez, A.; Sparrow, D.B.; Iyer, K.R.; Greasby, J.A.; Sheng, D.; Dunwoodie, S.L.; Chapman, G.; Humphreys, D.T.; Ip, E.; Giannoulatou, E.; McInerney-Leo, A.M.; Leo, P.J.; Duncan, E.L.; Wohler, E.; Sobreira, N.L.M.; Dimartino, C.; Amiel, J.; Gordon, C.T.; Capri, Y.; Lehalle, D.; Mory, A.; Wilnai, Y.; Baris Feldman, H.; Lebenthal, Y.; Gharavi, A.G.; Milo Rasouly, H.; Krzemień, G.G.; Miklaszewska, M.; Steiner, R.D.; Raggio, C.; Blank, R.; Jobling, R.; Giampietro, P.F.
Source
In: Human Molecular Genetics . (Human Molecular Genetics, 15 November 2020, 29(22):3662-3678)
Subject
Language
English
ISSN
14602083
09646906
09646906