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FENDO.2017.00064
FENDO.2017.00064
http://dx.doi.org/10.3389/FENDO.2017.00064
A Novel TBX19 Gene Mutation in a Case of Congenital Isolated Adrenocorticotropic Hormone Deficiency Presenting with Recurrent Respiratory Tract Infections.
P356
Q40231818-F21F4E90-2AB3-43D4-87B9-D0B4B7C018F7
P356
FENDO.2017.00064
http://dx.doi.org/10.3389/FENDO.2017.00064