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Mutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2

✍ Scribed by Metherell, Louise A; Chapple, J Paul; Cooray, Sadani; David, Alessia; Becker, Christian; Rüschendorf, Franz; Naville, Danielle; Begeot, Martine; Khoo, Bernard; Nürnberg, Peter

Book ID: 109919105
Publisher: Nature Publishing Group
Year: 2005
Tongue: English
Weight: 236 KB
Volume: 37
Category: Article
ISSN: 1061-4036
DOI: 10.1038/ng1501

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