Mutations in the Chromatin Regulator Gene BRPF1 Cause Syndromic Intellectual Disability and Deficient Histone Acetylation
- Author(s):
- Yan, K.Z.; Rousseau, J.; Littlejohn, R.O.; Kiss, C.; Lehman, A.; Rosenfeld, J.A.; Stumpel, C.T.R.; Stegmann, A.P.A.; Robak, L.; Scaglia, F.; Nguyen, T.T.M.; Fu, H.; Ajeawung, N.F.; Camurri, M.V.; Li, L.; Gardham, A.; Panis, B.; Almannai, M.; Sacoto, M.J.G.; Baskin, B.; Ruivenkamp, C.; Xia, F.; Bi, W.; Cho, M.T.; Potjer, T.P. (0000-0002-3831-6022); Santen, G.W.E. (0000-0003-1959-3267); Parker, M.J.; Canham, N.; McKinnon, M.; Potocki, L.; MacKenzie, J.J.; Roeder, E.R.; Campeau, P.M.; Yang, X.J.; DDD Study; CAUSES Study
- Published
- 2017
- Publication type
- Article / Letter to editor
- Date issued
- 2017-01-05
- Language
- English
- Is part of
- American Journal of Human Genetics (2017), Vol. 100, no. 1, p. 91-104
- hdl
- 1887/114684
- doi
- 10.1016/j.ajhg.2016.11.011
