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Q40561484-17A55BFC-1785-4F76-9049-3C50108613FE
Q40561484-17A55BFC-1785-4F76-9049-3C50108613FE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40561484-17A55BFC-1785-4F76-9049-3C50108613FE
A novel deletion mutation in IL2RG gene results in X-linked severe combined immunodeficiency with an atypical phenotype.
P2860
Q40561484-17A55BFC-1785-4F76-9049-3C50108613FE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40561484-17A55BFC-1785-4F76-9049-3C50108613FE
rank
NormalRank
type
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Statement
wasDerivedFrom
1fcf6d68968d050145316e2b54e89d60aac3ab59
P2860
Clinical and immunological manifestations of patients with atypical severe combined immunodeficiency.