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Omenn syndrome due to mutation of the RAG2 gene.
Published in:
2009
By:
Ktiouet, S;
Bertrand, Y;
Rival-Tringali, AL;
Kanitakis, J;
Malcus, C;
Poitevin, F;
Picard, C;
Claudy, A;
Faure, M
Publication type:
Letter
