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Functional relationships between three novel homozygous mutations in the ACTH receptor gene and familial glucocorticoid deficiency

✍ Scribed by A. Penhoat; D. Naville; H. El Mourabit; A. Buronfosse; M. Berberoglu; G. Ocal; C. Tsigos; P. Durand; M. Bégeot

Publisher: Springer
Year: 2002
Tongue: English
Weight: 131 KB
Volume: 80
Category: Article
ISSN: 0946-2716
DOI: 10.1007/s00109-002-0333-7

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