Mutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2
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F. Rüschendorf | C. Becker | P. Nürnberg | L. Metherell | A. David | B. Khoo | M. Cheetham | A. Huebner | D. Naville | A. Clark | M. Bégeot | J. Chapple | S. Cooray