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Q30492620-4A375BD3-21E8-4711-88AA-7A09E59F6989
Q30492620-4A375BD3-21E8-4711-88AA-7A09E59F6989
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30492620-4A375BD3-21E8-4711-88AA-7A09E59F6989
A novel form of cell type-specific partial IFN-gammaR1 deficiency caused by a germ line mutation of the IFNGR1 initiation codon.
P31
Q30492620-4A375BD3-21E8-4711-88AA-7A09E59F6989
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30492620-4A375BD3-21E8-4711-88AA-7A09E59F6989
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
1b83765ca0674305ecbf324861610d4e64defa4c
P31
scholarly article