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DDP507
DDP507
http://dx.doi.org/10.1093/HMG/DDP507
A novel form of cell type-specific partial IFN-gammaR1 deficiency caused by a germ line mutation of the IFNGR1 initiation codon.
P356
Q30492620-655A379D-651C-4E74-AC0C-56AE7B4BC2C8
P356
DDP507
http://dx.doi.org/10.1093/HMG/DDP507