A novel form of cell type-specific partial IFN-γR1 deficiency caused by a germ line mutation of the IFNGR1 initiation codon

由 Kong, Xiao-Fei, Vogt, Guillaume, Chapgier, Ariane, Lamaze, Christophe, Bustamante, Jacinta, Prando, Carolina, Fortin, Anny, Puel, Anne, Feinberg, Jacqueline, Zhang, Xin-Xin, Gonnord, Pauline, Pihkala-Saarinen, Ulla M., Arola, Mikko, Moilanen, Petra, Abel, Laurent, Korppi, Matti, Boisson-Dupuis, Stéphanie, Casanova, Jean-Laurent
出版 2010