De novo variants in CNOT3 cause a variable neurodevelopmental disorder
| Title: | De novo variants in CNOT3 cause a variable neurodevelopmental disorder |
|---|---|
| Authors: | Martin, R.Aff1, cor1; Splitt, M.Aff1; Genevieve, D.Aff2; Aten, E.Aff3; Collins, A.Aff4; de Bie, C. I.Aff5; Faivre, L.Aff6; Foulds, N.Aff4; Giltay, J.Aff5; Ibitoye, R.Aff4; Joss, S.Aff7; Kennedy, J.Aff8; Kerr, B.Aff9; Kivuva, E.Aff10; Koopmans, M.Aff3; Newbury-Ecob, R.Aff8; Jean-Marçais, N.Aff6; Peeters, E. A. J.Aff11; Smithson, S.Aff8; Tomkins, S.Aff8; Tranmauthem, F.Aff6; Piton, A.Aff12; van Haeringen, A.Aff3 |
| Source: | European Journal of Human Genetics. 27(11):1677-1682 |
| Database: | Springer Nature Journals |