Homozygous nonsense and frameshift mutations of the ACTH receptor in children with familial glucocorticoid deficiency (FGD) are not associated with long-term mineralocorticoid deficiency
View/ Open
Volume
71
Pagination
171 - 175
DOI
10.1111/j.1365-2265.2008.03511.x
Journal
CLIN ENDOCRINOL
Issue
ISSN
0300-0664
Metadata
Show full item recordAuthors
Chan, LF; Metherell, LA; Krude, H; Ball, C; O'Riordan, SMP; Costigan, C; Lynch, SA; Savage, MO; Cavarzere, P; Clark, AJLCollections
- Centre for Endocrinology [527]