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s00251-016-0949-3
s00251-016-0949-3
https://scigraph.springernature.com/pub.10.1007/s00251-016-0949-3
A novel deletion mutation in IL2RG gene results in X-linked severe combined immunodeficiency with an atypical phenotype.
P2888
Q40561484-CDCC79FF-3C9B-44AA-9596-F2621C0D6FD4
P2888
s00251-016-0949-3
https://scigraph.springernature.com/pub.10.1007/s00251-016-0949-3