De novo variants in CNOT3 cause a variable neurodevelopmental disorder
Martin, R., Splitt, M., Genevieve, D., Aten, E., Collins, A., de Bie, C. I., Faivre, L., Foulds, N., Giltay, J., Ibitoye, R., Joss, S., Kennedy, J., Kerr, B., Kivuva, E., Koopmans, M., Newbury-Ecob, RLanguage:
english
Journal:
European Journal of Human Genetics
DOI:
10.1038/s41431-019-0413-6
Date:
June, 2019
File:
PDF, 622 KB
english, 2019