Expanding the mutation spectrum in ICF syndrome: Evidence for a gender bias in ICF2

Author(s):
Boogaard, M.L. van den; Thijssen, P.E.; Aytekin, C.; Licciardi, F.; Kiykim, A.A.; Spossito, L.; Dalm, V.A.S.H.; Driessen, G.J.; Kersseboom, R.; Vries, F. de; Ostaijen-ten Dam, M.M. van; Ikinciogullari, A.; Dogu, F.; Oleastro, M.; Bailardo, E.; Daxinger, L.; Nain, E.; Baris, S.; Tol, M.J.D. van (0000-0003-1600-4279); Weemaes, C.; Maarel, S.M. van der (0000-0001-8103-711X)
Published
2017
Publication type
Article / Letter to editor
DNMT3BICF syndromeimmunodeficiencyZBTB24
Date issued
2017-10-31
Language
English
Is part of
Clinical Genetics (2017), Vol. 92, no. 4, p. 380-387
hdl
1887/94623
doi
10.1111/cge.12979