Congenital adrenal hyperplasia due to 11 β-hydroxylase deficiency: Clinical, Biochemical and Genetic characteristics

被引：0
|
作者：
Ladjouze, Asmahane [1 ,2 ]
Mohammedi, Kahina [2 ,3 ]
Demdoum, Mohamed [4 ]
Boulesnane, Kamelia [1 ,2 ]
Aboura, Rawda [1 ,2 ]
Melzi, Souhila [1 ,2 ]
Bouhafs, Nadjet [1 ,2 ]
Donaldson, Malcolm [5 ]
Janot, Clement [6 ]
Mallet, Delphine [6 ]
Bouzerar, Zair [1 ,2 ]
Roucher-Boulez, Florence [6 ]
机构：
[1] CHU Bab El Oued, Serv Pediat, Algiers, Algeria
[2] Fac Med Alger, Algiers, Algeria
[3] EPH Ain Taya, Serv Pediat, Algiers, Algeria
[4] Cabinet Liberal, El Oued, Algeria
[5] Queen Elizabeth Univ Hosp, Sch Med, Sect Child Hlth 3, Glasgow, Lanark, Scotland
[6] Univ Lyon1, Hosp Civils Lyon, Mol Endocrinol & Rare Dis, Lyon, France
来源：
HORMONE RESEARCH IN PAEDIATRICS | 2023年 / 96卷
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
P1-406
引用
收藏
页码：154 / 154
页数：1
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