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A novel form of cell type-specific partial IFN-γR1 deficiency caused by a germ line mutation of the IFNGR1 initiation codon
Xiao Fei Kong, Guillaume Vogt, Ariane Chapgier, Christophe Lamaze, Jacinta Bustamante, Carolina Prando, Anny Fortin, Anne Puel, Jacqueline Feinberg, Xin Xin Zhang, Pauline Gonnord, Ulla M. Pihkala-Saarinen, Mikko Arola, Petra Moilanen, Laurent Abel, Matti Korppi, Stéphanie Boisson-Dupuis, Jean Laurent Casanova
Research output: Contribution to journal › Article › peer-review
36
Scopus
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