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：

引用

页码：589 / &

共 62 条

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