학술논문
De novo variants in CNOT3 cause a variable neurodevelopmental disorder
Document Type
Article
Author
Martin, R.; Splitt, M.; Genevieve, D.; Aten, E.; Koopmans, M.; van Haeringen, A.; Collins, A.; Foulds, N.; Ibitoye, R.; de Bie, C.I.; Giltay, J.; Faivre, L.; Jean-Marçais, N.; Tranmauthem, F.; Joss, S.; Kennedy, J.; Newbury-Ecob, R.; Smithson, S.; Tomkins, S.; Kerr, B.; Kivuva, E.; Peeters, E.A.J.; Piton, A.
Source
In: European Journal of Human Genetics . (European Journal of Human Genetics, 1 November 2019, 27(11):1677-1682)
Subject
Language
English
ISSN
14765438
10184813
10184813