Case Report
Published on 18 Apr 2019
A Case of Congenital Isolated Adrenocorticotropic Hormone Deficiency Caused by Two Novel Mutations in the TBX19 Gene
in Pituitary Endocrinology
Frontiers in Endocrinology
doi 10.3389/fendo.2019.00251
- 4,447 views
- 14 citations


