NEW HEREDITARY DEFECT IN BIOSYNTHESIS OF ALDOSTERONE - URINARY C21-CORTICOSTEROID PATTERN IN 3 RELATED PATIENTS WITH SALT-LOSING SYNDROME SUGGESTING 18-OXIDATION DEFECT

被引:114
作者
VISSER, HKA
COST, WS
机构
来源
ACTA ENDOCRINOLOGICA | 1964年 / 47卷 / 04期
关键词
D O I
10.1530/acta.0.0470589
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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页码:589 / &
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