No clinical signs of Hyper-IgM or other relevant primary immunodeficiency syndrome in novel patients with constitutional mismatch repair deficiency (CMMRD)

Author(s):
Tesch, V.K.; Raicht, A.; Ijspeert, H.; Rueda-Fernandez, D.; Colas, C.; Kuerten, T.; Ilencikova, D.; Hezam, I.; Feldman, H.B.; Nathrath, M.; Suerink, M.; Januszkiewicz-Lewandowska, D.; Ragab, I.; Azizi, A.; Schwinger, W.; Vanderburg, M.; Brugieres, L.; Wimmer, K.; Seidel, M.G.
Published
2018
Publication type
Article / Letter to editor
Date issued
2018-04-30
Language
English
Is part of
Journal of Clinical Immunology (2018), Vol. 38, no. 3, p. 387-387
hdl
1887/3195318