Identification of a novel non-coding mutation in C1qB in a Dutch child with C1q deficiency associated with recurrent infections

Author(s):
Schaarenburg, R.A. van; Daha, N.A.; Schonkeren, J.J.M.; Levarht, E.W.N.; Gijlswijk-Janssen, D.J. van; Kurreeman, F.A.S.; Roos, A.; Kooten, C. van (0000-0002-6257-0899); Koelman, C.A.; Ernst-Kruis, M.R.; Toes, R.E.M.; Huizinga, T.W.J.; Lankester, A.C.; Trouw, L.A. (0000-0001-5186-2290)
Published
2015
Publication type
Article / Letter to editor
AutoimmunityComplementC1q deficiencyInfectionsMutationPrimary immunodeficiency
Date issued
2015-03-31
Language
English
Is part of
Immunobiology (2015), Vol. 220, no. 3, p. 422-427
hdl
1887/113674
doi
10.1016/j.imbio.2014.10.005