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

Schaarenburg, R.A. van; Daha, N.A.; Schonkeren, J.J.M.; Levarht, E.W.N.; Gijlswijk-Janssen, D.J. van; Kurreeman, F.A.S.; ... ; Trouw, L.A. (2015)

Article / Letter to editor

• Autoimmunity
• Complement
• C1q deficiency
• Infections
• Mutation
• Primary immunodeficiency

• All authors: 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; Koelman, C.A.; Ernst-Kruis, M.R.; Toes, R.E.M.; Huizinga, T.W.J.; Lankester, A.C.; Trouw, L.A.
• Date: 2015-03-31
• Journal: Immunobiology
• Volume: 220
• Issue: 3
• Pages: 422 - 427
• DOI: doi:10.1016/j.imbio.2014.10.005