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Q40561484-56B2DA1A-6755-4B16-8860-E35B997FCB8B
Q40561484-56B2DA1A-6755-4B16-8860-E35B997FCB8B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40561484-56B2DA1A-6755-4B16-8860-E35B997FCB8B
A novel deletion mutation in IL2RG gene results in X-linked severe combined immunodeficiency with an atypical phenotype.
P2860
Q40561484-56B2DA1A-6755-4B16-8860-E35B997FCB8B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40561484-56B2DA1A-6755-4B16-8860-E35B997FCB8B
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Statement
wasDerivedFrom
1fcf6d68968d050145316e2b54e89d60aac3ab59
P2860
A novel mutant gammac chain from a patient with typical phenotype of X-linked severe combined immunodeficiency (SCID) has partial signalling function for mediating IL-2 and IL-4 receptor action.