A purely quantitative form of partial recessive IFN-γR2 deficiency caused by mutations of the initiation or second codon.
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Oleaga-Quintas C, et al. Among authors: gulhan b.
Hum Mol Genet. 2018 Nov 15;27(22):3919-3935. doi: 10.1093/hmg/ddy275.
Hum Mol Genet. 2018.
PMID: 31222290
Free PMC article.