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    Daphne Heijsman
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    Journal Articles

    Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndrome

    In Special Collection:
    Monogenic Auto-Inflammation and Auto-Immunity in Humans 2018
    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
    Journal: Journal of Experimental Medicine
    J Exp Med (2016) 213 (7): 1163–1174.
    https://doi.org/10.1084/jem.20151529
    Published: 20 June 2016
    View article titled, Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndrome
    Open the PDF for Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndrome in another window
    Includes: Supplementary data

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