Homozygous nonsense and frameshift mutations of the ACTH receptor in children with familial glucocorticoid deficiency (FGD) are not associated with long-term mineralocorticoid deficiency

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Volume
71
Pagination
171 - 175
DOI
10.1111/j.1365-2265.2008.03511.x
Journal
CLIN ENDOCRINOL
Issue
2
ISSN
0300-0664
Metadata
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Authors
Chan, LF; Metherell, LA; Krude, H; Ball, C; O'Riordan, SMP; Costigan, C; Lynch, SA; Savage, MO; Cavarzere, P; Clark, AJL
URI
http://qmro.qmul.ac.uk/xmlui/handle/123456789/18040
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Licence information
Creative Commons Deed, Attribution 2·5, which does not permit commercial exploitation.
Copyright statements
2009. The authors