Genetics of ACTH insensitivity syndromes

Annales d'Endocrinologie

Volumn 66, Issue 3, 2005, Pages 247-249

  Clark, J L A ^a   Metherell, L A ^a   Naville, D ^b   Begeot, M ^b   Huebner, A ^c  

^a QUEEN MARY UNIVERSITY OF LONDON   (United Kingdom)

^b INSERM   (France)

^c DRESDEN UNIVERSITY OF TECHNOLOGY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CORTICOTROPIN; CORTICOTROPIN RECEPTOR; GLUCOCORTICOID;

ALLGROVE SYNDROME; AUTOSOMAL RECESSIVE INHERITANCE; CELL STIMULATION; CLINICAL FEATURE; CONFERENCE PAPER; CORTICOTROPIN BLOOD LEVEL; DIFFERENTIAL DIAGNOSIS; GENE MAPPING; GENE MUTATION; GENETIC ANALYSIS; GLUCOCORTICOSTEROID DEFICIENCY; HORMONE DEFICIENCY; HUMAN; PATHOGENESIS;

EID: 18944397267     PISSN: 00034266     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0003-4266(05)81757-3     Document Type: Conference Paper

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