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

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Description scientific article
Author/s

author: Lou Metherell  Adrian J. L. Clark  Michael E. Cheetham  Danielle Naville  Christian Becker  Peter Nürnberg  Franz Rüschendorf 

Publication date February 2005
Language English
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