Linkage analysis of familial hyperaldosteronism type II - Absence of linkage to the gene encoding the angiotensin II receptor type 1 [6]

Journal of Clinical Endocrinology and Metabolism

Volumn 83, Issue 3, 1998, Pages 1046-

  Torpy, D J ^a   Stratakis, C A ^a   Gordon, R D ^a  

^a EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH AND HUMAN DEVELOPMENT   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALDOSTERONE; ANGIOTENSIN; ANGIOTENSIN 1 RECEPTOR; DEXAMETHASONE; DNA; GLUCOCORTICOID;

CLINICAL ARTICLE; DEXAMETHASONE SUPPRESSION TEST; FAMILIAL DISEASE; FEMALE; GENETIC LINKAGE; HUMAN; LETTER; MALE; PEDIGREE ANALYSIS; PRIMARY HYPERALDOSTERONISM; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM; SOMATIC MUTATION;

FEMALE; HUMANS; HYPERALDOSTERONISM; LINKAGE (GENETICS); MALE; PEDIGREE; RECEPTORS, ANGIOTENSIN;

EID: 0031792526     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jc.83.3.1046     Document Type: Letter

References (5)