Back to matchesWe found a matchYour institution may have rights to this item. Sign in to continue.TitleA novel form of cell type-specific partial IFN-γR1 deficiency caused by a germ line mutation of the IFNGR1 initiation codon.AuthorsKong, 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-LaurentPublicationHuman Molecular Genetics, 2010, Vol 19, Issue 3, p434ISSN0964-6906Publication typeArticleDOI10.1093/hmg/ddp507