ACTH receptor gene mutations and hereditary glucocorticoid deficiency;MUTATIONS DU GENE DU RECEPTEUR A L'ACTH ET SYNDROME FAMILIAL DE DEFICIT EN GLUCOCORTICOIDES

Annales d'Endocrinologie

Volumn 57, Issue 2, 1996, Pages 101-106

  Naville, D ^a   Barjhoux, L ^a   Jaillard, C ^a   Faury, D ^a   Despert, F ^b   Esteva, B ^c   Durand, Ph ^a   Saez, J ^a   Begeot, M ^a  

^a HÔPITAL DEBROUSSE   (France)

^b Centre de Pediatrie Clocheville   (France)

^c ARMAND TROUSSEAU HOSPITAL   (France)

Author keywords

ACTH receptor; glucocorticoid deficiency

Indexed keywords

CORTICOTROPIN RECEPTOR; CYCLIC AMP; GLUCOCORTICOID;

GLUCOCORTICOSTEROID DEFICIENCY; HORMONE DEFICIENCY; HUMAN; HUMAN TISSUE; MOLECULAR BIOLOGY; MUTATION; SHORT SURVEY; ARTICLE; CASE REPORT; GENE EXPRESSION; GENETICS; IN VITRO STUDY; INFANT; METABOLISM; NEWBORN; SYNDROME;

GENE EXPRESSION; GLUCOCORTICOIDS; HUMANS; INFANT; INFANT, NEWBORN; MUTATION; RECEPTORS, CORTICOTROPIN; SYNDROME;

EID: 0029951589     PISSN: 00034266     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Short Survey

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