Molecular basis for hypertension in the 'type II variant' of apparent mineralocorticoid excess

American Journal of Human Genetics

Volumn 63, Issue 2, 1998, Pages 370-379

  Li, A ^a   Tedde, R ^b   Krozowski, Z S ^c   Pala, A ^b   Li, K X Z ^c   Shackleton, C H L ^d   Mantero, F ^e   Palermo, M ^b   Stewart, P M ^a  

^a UNIVERSITY DEPARTMENT OF MEDICINE   (United Kingdom)

^b UNIVERSITY OF SASSARI   (Italy)

^c BAKER IDI HEART AND DIABETES INSTITUTE   (Australia)

^d CHILDREN S HOSPITAL OAKLAND   (United States)

^e UNIVERSITÀ POLITECNICA DELLE MARCHE   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

11BETA HYDROXYSTEROID DEHYDROGENASE; CORTISONE; HYDROCORTISONE; MINERALOCORTICOID;

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; CHILD; CLINICAL ARTICLE; DISEASE CLASSIFICATION; DISEASE SEVERITY; ENZYME ACTIVITY; FEMALE; GENETIC LINKAGE; HUMAN; HYPERTENSION; MALE; POINT MUTATION; PRIORITY JOURNAL; STEROID METABOLISM;

EID: 0032231654     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/301955     Document Type: Article

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