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Li F. Chan, Louise A. Metherell, Heiko Krude, Colin Ball, Stephen M. P. O'Riordan, Colm Costigan, Sally A. Lynch, Martin O. Savage, Paolo Cavarzere and Adrian J. L. Clark Homozygous nonsense and frameshift mutations of the ACTH receptor in children with familial glucocorticoid deficiency (FGD) are not associated with long-term mineralocorticoid deficiency Clinical Endocrinology 71

Version of Record online: 17 DEC 2008 | DOI: 10.1111/j.1365-2265.2008.03511.x

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