Congenital adrenal hyperplasia caused by compound heterozygosity of two novel CYP11B1 gene variants

被引：0
|
作者：
I. Fylaktou
P. Smyrnaki
A. Sertedaki
M. Dracopoulou
Ch. Kanaka-Gantenbein
机构：
[1] National and Kapodistrian University of Athens,Division of Endocrinology, Diabetes and Metabolism, Center for Rare Paediatric Endocrine Diseases, First Department of Paediatrics, Medical School
[2] Agia Sophia” Children’s Hospital,undefined
来源：
Hormones | 2022年 / 21卷
关键词：
Congenital adrenal hyperplasia; 11β-hydroxylase deficiency; gene mutations;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
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页码：155 / 161
页数：6
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