A Novel Point Mutation in the Amino Terminal Domain of the Human Glucocorticoid Receptor (hGR) Gene Enhancing hGR-Mediated Gene Expression

Context: Interindividual variations in glucocorticoid sensitivity have been associated with manifestations of cortisol excess or deficiency and may be partly explained by polymorphisms in the human glucocorticoid receptor (hGR) gene. We studied a 43-yr-old female, who presented with manifestations c...

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Autores principales: Charmandari, Evangelia, Ichijo, Takamasa, Jubiz, William, Baid, Smita, Zachman, Keith, Chrousos, George P., Kino, Tomoshige
Formato: Artigo
Lenguaje:Inglês
Publicado: The Endocrine Society 2008
Materias:
Brief Report
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC2626453/
https://ncbi.nlm.nih.gov/pubmed/18827003
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2008-0892
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