Clinical case seminar: Type 1 aldosterone synthase deficiency presenting in a middle-aged man

Journal of Clinical Endocrinology and Metabolism

Volumn 86, Issue 3, 2001, Pages 1008-1012

  Kayes Wandover, Kathleen M ^a   Lee Schindler, R E ^a   Taylor, Harris C ^b   White, Perrin C ^a  

^a UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

^b FAIRVIEW HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

18 HYDROXYCORTICOSTERONE; ALDOSTERONE SYNTHASE; GENE PRODUCT; ALDOSTERONE; RENIN;

ADULT; ALDOSTERONE BLOOD LEVEL; AMINO ACID SEQUENCE; CASE REPORT; CLINICAL FEATURE; CODON; CONFERENCE PAPER; ELECTROLYTE DISTURBANCE; ENZYME DEFICIENCY; EXON; FAILURE TO THRIVE; FAMILY HISTORY; GENE DUPLICATION; GENE INSERTION; GENE MUTATION; GENETIC ANALYSIS; HOMOZYGOSITY; HUMAN; LABORATORY DIAGNOSIS; MALE; ONSET AGE; PRIORITY JOURNAL; ARTICLE; BLOOD; GENETIC TRANSFECTION; GENETICS; HOMOZYGOTE; MUTATION; URINE;

18-HYDROXYCORTICOSTERONE; ALDOSTERONE; ALDOSTERONE SYNTHASE; CODON; EXONS; GENE DUPLICATION; HOMOZYGOTE; HUMANS; MALE; MUTATION; RENIN; TRANSFECTION;

EID: 0035290801     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jc.86.3.1008     Document Type: Conference Paper

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