Congenital erythroderma should be considered as an urgent warning sign of immunodeficiency: A case of Omenn syndrome

E. Cuperus, J.M. van Montfrans (Joris), M. van Gijn (Marielle), M.T. Bastiaens (Maarten), de Willigen, M.M.A. (Mirjam M. A.), P. Leguit (Piet), Brijnzeel-Koomen, C.A.F.M. (Carla A. F. M.), Russel, I.M.B. (Ingrid M. B.) and S.G.M.A. Pasmans (Suzanne)

2017-05-01

European Journal of Dermatology , Volume 27 - Issue 3 p. 313- 314

Additional Metadata
Persistent URL	doi.org/10.1684/ejd.2017.2992, hdl.handle.net/1765/108425
Journal	European Journal of Dermatology
Rights	no subscription
Organisation	Erasmus MC: University Medical Center Rotterdam
Citation APA Style AAA Style APA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style American-Institute-of-Physics Style Council-of-Science-Editors Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format	Cuperus, E., van Montfrans, J., van Gijn, M., Bastiaens, M., de Willigen, M.M.A. (Mirjam M. A.), Leguit, P., … Pasmans, S. (2017). Congenital erythroderma should be considered as an urgent warning sign of immunodeficiency: A case of Omenn syndrome. European Journal of Dermatology, 27(3), 313–314. doi:10.1684/ejd.2017.2992

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