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1 Ergebnisse
1
Human USP18 deficiency underlies type 1 interferonopathy le..:
Meuwissen, Marije E.C
;
Schot, Rachel
;
Buta, Sofija
...
info:eu-repo/semantics/altIdentifier/doi/10.1084/jem.20151529. , 2016
Link:
https://pasteur.hal.science/pasteur-02070980
RT Journal T1
Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndrome
UL https://suche.suub.uni-bremen.de/peid=base-ftinstpasteur:oai:HAL:pasteur-02070980v1&Exemplar=1&LAN=DE A1 Meuwissen, Marije E.C A1 Schot, Rachel A1 Buta, Sofija A1 Oudesluijs, Grétel A1 Tinschert, Sigrid A1 Speer, Scott A1 Li, Zhi A1 van Unen, Leontine A1 Heijsman, Daphne A1 Goldmann, Tobias A1 Lequin, Maarten A1 Kros, Johan A1 Stam, Wendy A1 Hermann, Mark A1 Willemsen, Rob A1 Brouwer, Rutger W.W A1 van Ijcken, Wilfred F.J A1 Martin-Fernandez, Marta A1 de Coo, Irenaeus A1 Dudink, Jeroen A1 de Vries, Femke A.T A1 Bertoli Avella, Aida A1 Prinz, Marco A1 Crow, Yanick A1 Verheijen, Frans A1 Pellegrini, Sandra A1 Bogunovic, Dusan A1 Mancini, Grazia M.S PB HAL CCSD; Rockefeller University Press YR 2016 K1 MESH: Autoimmune Diseases of the Nervous System K1 MESH: Brain K1 MESH: Nervous System Malformations K1 MESH: Signal Transduction K1 MESH: Calcinosis K1 MESH: Endopeptidases K1 MESH: Female K1 MESH: Humans K1 MESH: Immunity K1 Innate K1 MESH: Interferon Type I K1 MESH: Male K1 MESH: Microglia K1 [SDV.GEN]Life Sciences [q-bio]/Genetics K1 [SDV.IMM]Life Sciences [q-bio]/Immunology JF info:eu-repo/semantics/altIdentifier/doi/10.1084/jem.20151529 LK http://dx.doi.org/https://pasteur.hal.science/pasteur-02070980 DO https://pasteur.hal.science/pasteur-02070980 SF ELIB - SuUB Bremen
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