Two rare forms of congenital adrenal hyperplasia, 11β hydroxylase deficiency and 17-hydroxylase/17,20-lyase deficiency, presenting with novel mutations

被引：0
作者：
Krupali Bulsari
Louise Maple-Brown
Henrik Falhammar
机构：
[1] Royal Darwin Hospital,Department of Endocrinology
[2] Princess Alexandra Hospital,Department of Endocrinology
[3] Menzies School of Health Research,Department of Endocrinology, Metabolism and Diabetes
[4] Karolinska University Hospital,Department of Molecular Medicine and Surgery
[5] Karolinska Institutet,undefined
来源：
Hormones | 2018年 / 17卷
关键词：
11 Beta-hydroxylase deficiency; 17-Hydroxylase/17,20-lyase deficiency; Congenital adrenal hyperplasia; Fertility; Long-term outcome;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
引用
收藏
页码：127 / 132
页数：5
相关论文
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