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Mutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2
Metherell, Louise A, Chapple, J Paul, Cooray, Sadani, David, Alessia, Becker, Christian, Rüschendorf, Franz, Naville, Danielle, Begeot, Martine, Khoo, Bernard, Nürnberg, PeterVolume:
37
Year:
2005
Language:
english
Pages:
5
DOI:
10.1038/ng1501
File:
PDF, 236 KB
english, 2005