Publication
Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndrome
Marije E.C. Meuwissen, Rachel Schot, Sofija Buta, Grétel Oudesluijs, Sigrid Tinschert, Scott D. Speer, Zhi Li, Leontine van Unen, Daphne Heijsman, Tobias Goldmann, Maarten H. Lequin, Johan M. Kros, Wendy Stam, Mark Hermann, Rob Willemsen, Rutger W.W. Brouwer, Wilfred F.J. Van IJcken, Marta Martin-Fernandez, Irenaeus de Coo, Jeroen Dudink, Femke A.T. de Vries, Aida Bertoli Avella, Marco Prinz, Yanick J. Crow, Frans W. Verheijen, Sandra Pellegrini, Dusan Bogunovic, Grazia M.S. Mancini
The Journal of Experimental Medicine, June 2016, Rockefeller University Press
DOI: 10.1084/jem.20151529