Mutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucorticoid deficiency type 2
2005
Metherell, L.A. | Chapple, J.P. | Cooray, S. | David, A. | Becker, C. | Ruschendorf, F. | Naville, D. | Bégeot, Martine | Khoo, B. | Nürnberg, P. | Huebner, A. | Cheetham, M.E. | Clark, A.J.L.
Bibliographic information
Other Subjects
Surrenale; [info] computer science [cs]; Glucortocoide; Genetique
Language
English
Type
Journal Article; Journal Part
Source
Nature Publishing Group
2021-03-15
AGRIS AP
Data Provider
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