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S00251-016-0949-3
S00251-016-0949-3
http://dx.doi.org/10.1007/S00251-016-0949-3
A novel deletion mutation in IL2RG gene results in X-linked severe combined immunodeficiency with an atypical phenotype.
P356
Q40561484-4BA3517E-00B2-458A-B60A-055D23D15518
P356
S00251-016-0949-3
http://dx.doi.org/10.1007/S00251-016-0949-3