Functional characterization of naturally occurring mutations of the human adrenocorticotropin receptor: Poor correlation of phenotype and genotype

Journal of Clinical Endocrinology and Metabolism

Volumn 84, Issue 8, 1999, Pages 2766-2770

  Elias, Lucila L K ^a   Huebner, Angela ^b   Pullinger, Gill D ^a   Mirtella, Adriana ^a   Clark, Adrian J L ^a  

^a ST BARTHOLOMEW S HOSPITAL   (United Kingdom)

^b DRESDEN UNIVERSITY OF TECHNOLOGY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CORTICOTROPIN RECEPTOR;

ARTICLE; BINDING AFFINITY; CHILD; CLINICAL FEATURE; CONCENTRATION RESPONSE; DISEASE SEVERITY; ENZYME ANALYSIS; GENE EXPRESSION; GENOTYPE; HORMONE DEFICIENCY; HORMONE RECEPTOR INTERACTION; HUMAN; HUMAN CELL; IC 50; INFANT; MISSENSE MUTATION; NEWBORN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN STRUCTURE;

EID: 0033306879     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jc.84.8.2766     Document Type: Article

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