Corticosteroid-binding globulin gene polymorphisms: Clinical implications and links to idiopathic chronic fatigue disorders

Clinical Endocrinology

Volumn 67, Issue 2, 2007, Pages 161-167

  Torpy, D J ^a   Ho, J T ^a  

^a ROYAL ADELAIDE HOSPITAL   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

HYDROCORTISONE; TRANSCORTIN;

BINDING AFFINITY; CHRONIC FATIGUE SYNDROME; DISEASE ASSOCIATION; DNA POLYMORPHISM; FATIGUE; GENE MUTATION; GENETIC ENGINEERING; GENETIC VARIABILITY; HORMONE BLOOD LEVEL; HORMONE DEFICIENCY; HORMONE TRANSPORT; HUMAN; HYDROCORTISONE BLOOD LEVEL; HYPOTENSION; IDIOPATHIC DISEASE; INSULIN RESISTANCE; NONHUMAN; OBESITY; PHENOTYPE; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN INTERACTION; REVIEW; TISSUE SPECIFICITY;

ANIMALS; FATIGUE SYNDROME, CHRONIC; GENETIC PREDISPOSITION TO DISEASE; HUMANS; HYDROCORTISONE; MICE; MICE, KNOCKOUT; MODELS, ANIMAL; POLYMORPHISM, GENETIC; TRANSCORTIN;

EID: 34447503556     PISSN: 03000664     EISSN: 13652265     Source Type: Journal    
DOI: 10.1111/j.1365-2265.2007.02890.x     Document Type: Review

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