Point mutation causing a single amino acid substitution in the hormone binding domain of the glucocorticoid receptor in familial glucocorticoid resistance.

Familial glucocorticoid resistance is a hypertensive, hyperandrogenic disorder characterized by increased serum cortisol concentrations in the absence of stigmata of Cushing's syndrome. Our previous studies of the first reported kindred showed a two- to threefold reduction in glucocorticoid rec...

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Detalhes bibliográficos
Main Authors: Hurley, D M, Accili, D, Stratakis, C A, Karl, M, Vamvakopoulos, N, Rorer, E, Constantine, K, Taylor, S I, Chrousos, G P
Formato: Artigo
Idioma:Inglês
Publicado em: 1991
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC296359/
https://ncbi.nlm.nih.gov/pubmed/1704018
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