A genetic defect resulting in mild low-renin hypertension

Proceedings of the National Academy of Sciences of the United States of America

Volumn 95, Issue 17, 1998, Pages 10200-10205

  Wilson, Robert C ^a   Dave Sharma, Swati ^a   Wei, Ji Qing ^a   Obeyesekere, Varuni R ^b   Li, Kevin ^b   Ferrari, Paolo ^c   Krozowski, Zygmunt S ^b   Shackleton, Cedric H L ^d   Bradlow, Leon ^a   Wiens, Timothy ^e   New, Maria I ^a  

^a WEILL CORNELL MEDICAL CENTER   (United States)

^b BAKER IDI HEART AND DIABETES INSTITUTE   (Australia)

^c UNIVERSITY OF BERN   (Switzerland)

^d CHILDREN S HOSPITAL OAKLAND   (United States)

^e Wichita Clinic   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

11BETA HYDROXYSTEROID DEHYDROGENASE; CORTISONE; HYDROCORTISONE; LEUCINE; MINERALOCORTICOID; PROLINE; RENIN;

ADULT; ANIMAL CELL; ARTICLE; CHILD; CLINICAL ARTICLE; ESSENTIAL HYPERTENSION; FAILURE TO THRIVE; FEMALE; GENE MUTATION; GROWTH RETARDATION; HUMAN; HYPOALDOSTERONISM; HYPOKALEMIC ALKALOSIS; INFANT; KIDNEY CALCIFICATION; LOW BIRTH WEIGHT; MALE; NONHUMAN; PRIORITY JOURNAL; RENIN ANGIOTENSIN ALDOSTERONE SYSTEM;

11-BETA-HYDROXYSTEROID DEHYDROGENASES; ADOLESCENT; BASE SEQUENCE; CHILD; CHILD, PRESCHOOL; CONSANGUINITY; CORTISONE; DNA MUTATIONAL ANALYSIS; DNA PRIMERS; FEMALE; HOMOZYGOTE; HUMANS; HYDROCORTISONE; HYDROXYSTEROID DEHYDROGENASES; HYPERTENSION; INFANT; MALE; METABOLISM, INBORN ERRORS; MINERALOCORTICOIDS; PEDIGREE; POINT MUTATION; RENIN;

ANIMALIA;

EID: 13144265720     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.95.17.10200     Document Type: Article

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