Mutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2
- 16 January 2005
- journal article
- letter
- Published by Springer Science and Business Media LLC in Nature Genetics
- Vol. 37 (2), 166-170
- https://doi.org/10.1038/ng1501
Abstract
No abstract availableKeywords
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