ACTH receptor mutation in a girl with familial glucocorticoid deficiency
- 1 January 1998
- journal article
- case report
- Published by Wiley in Clinical Genetics
- Vol. 53 (1) , 57-62
- https://doi.org/10.1034/j.1399-0004.1998.531530112.x
Abstract
Familial glucocorticoid deficiency (FGD) has long been recognised as a clinical entity, but molecular studies have so far been performed in only a few individuals. We describe a girl born to consangu...Keywords
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