Mutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2
published in: Nature Genetics
date of publication: 2005-02
language: English
main subject: glucocorticoid, glucocorticoid deficiency 2
Cites articles 20
- 1998-12-01
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Article - wd:Q28302878