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Q37002477-EE50DCD7-F70C-4167-B804-33F4EE9060FE
Q37002477-EE50DCD7-F70C-4167-B804-33F4EE9060FE
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Statement
http://www.wikidata.org/entity/statement/Q37002477-EE50DCD7-F70C-4167-B804-33F4EE9060FE
A RAG1 mutation found in Omenn syndrome causes coding flank hypersensitivity: a novel mechanism for antigen receptor repertoire restriction
P2860
Q37002477-EE50DCD7-F70C-4167-B804-33F4EE9060FE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37002477-EE50DCD7-F70C-4167-B804-33F4EE9060FE
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wasDerivedFrom
671591ea90c8e15e70eac1537d53a495d789bc43
P2860
Conditional RAG-1 mutants block the hairpin formation step of V(D)J recombination.