Mutations in CDC45, Encoding an Essential Component of the Pre-initiation Complex, Cause Meier-Gorlin Syndrome and Craniosynostosis

Author(s):: Fenwick, A.L.; Kliszczak, M.; Cooper, F.; Murray, J.; Sanchez-Pulido, L.; Twigg, S.R.F.; Goriely, A.; McGowan, S.J.; Miller, K.A.; Taylor, I.B.; Logan, C.; Bozdogan, S.; Danda, S.; Dixon, J.; Elsayed, S.M.; Elsobky, E.; Gardham, A.; Hoffer, M.J.V. (0000-0002-1812-7670); Koopmans, M.; McDonald-McGinn, D.M.; Santen, G.W.E.; Savarirayan, R.; Silva, D. de; Vanakker, O.; Wall, S.A.; Wilson, L.C.; Yuregir, O.O.; Zackai, E.H.; Ponting, C.P.; Jackson, A.P.; Wilkie, A.O.M.; Niedzwiedz, W.; Bicknell, L.S.; WGS500 Consortium

Date issued: 2016-07-07
Language: English
Is part of: American Journal of Human Genetics (2016), Vol. 99, no. 1, p. 125-138
hdl: 1887/112963
doi: 10.1016/j.ajhg.2016.05.019