Hereditary isolated glucocorticoid deficiency is associated with abnormalities of the adrenocorticotropin receptor gene.

Isolated glucocorticoid deficiency (IGD) is an autosomal recessive disorder characterized by progressive primary adrenal insufficiency, without mineralocorticoid deficiency. The cDNA and gene of the human ACTH receptor were recently cloned. The gene encodes a 297-amino acid protein that belongs to t...

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Detalhes bibliográficos

Publicado no:	J Clin Invest
Principais autores:	Tsigos, C, Arai, K, Hung, W, Chrousos, G P
Formato:	Artigo
Idioma:	Inglês
Publicado em:	American Society for Clinical Investigation 1993
Assuntos:	Research Article
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC288430/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8227361/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI116853
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