Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains
- Author(s):
- Geisheker, M.R.; Heymann, G.; Wang, T.Y.; Coe, B.P.; Turner, T.N.; Stessman, H.A.F.; Hoekzema, K.; Kvarnung, M.; Shaw, M.; Friend, K.; Liebelt, J.; Barnett, C.; Thompson, E.M.; Haan, E.; Guo, H.; Anderlid, B.M.; Nordgren, A.; Lindstrand, A.; Vandeweyer, G.; Alberti, A.; Avola, E.; Vinci, M.; Giusto, S.; Pramparo, T.; Pierce, K.; Nalabolu, S.; Michaelson, J.J.; Sedlacek, Z.; Santen, G.W.E. (0000-0003-1959-3267); Peeters, H.; Hakonarson, H.; Courchesne, E.; Romano, C.; Kooy, R.F.; Bernier, R.A.; Nordenskjold, M.; Gecz, J.; Xia, K.; Zweifel, L.S.; Eichler, E.E.
- Published
- 2017
- Publication type
- Article / Letter to editor
- Date issued
- 2017-08-31
- Language
- English
- Is part of
- Nature Neuroscience (2017), Vol. 20, no. 8, p. 1043-+
- hdl
- 1887/94670
- doi
- 10.1038/nn.4589
