A novel form of cell type-specific partial IFN-R1 deficiency caused by a germ line mutation of the IFNGR1 initiation codon

Author: 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 Stphanie   Casanova Jean-Laurent  

Publisher: Oxford University Press

ISSN: 1460-2083

Source: Human Molecular Genetics, Vol.19, Iss.3, 2010-02, pp. : 434-444

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