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Q38236321-077E7108-C923-4750-BE90-CF860F6D1880
Q38236321-077E7108-C923-4750-BE90-CF860F6D1880
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http://www.wikidata.org/entity/statement/Q38236321-077E7108-C923-4750-BE90-CF860F6D1880
Genetic defects in cytolysis in macrophage activation syndrome.
P2860
Q38236321-077E7108-C923-4750-BE90-CF860F6D1880
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38236321-077E7108-C923-4750-BE90-CF860F6D1880
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df82318203b1942c739d917ec0c1306b74f0210d
P2860
A functional analysis of the putative polymorphisms A91V and N252S and 22 missense perforin mutations associated with familial hemophagocytic lymphohistiocytosis.