Structure-function relationships in congenital adrenal hyperplasia due to 11-hydroxylase deficiency -: insights from two novel mutations (M92X, R453Q) in the CYP11B1 gene

被引：0
|
作者：
Krone, Nils
Groetzinger, Joachim
Holterhus, Paul Martin
Sippell, Wolfgang G.
Schwarz, Hans Peter
Riepe, Felix G.
机构：
[1] Univ Hosp Schleswig Holstein, Dept Paediat, Div Paed Endocrinol, Kiel, Germany
[2] Univ Kiel, Inst Biochem, D-2300 Kiel, Germany
[3] Univ Munich, Univ Childrens Hosp, Munich, Germany
来源：
HORMONE RESEARCH | 2006年 / 65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：
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收藏
页码：17 / 17
页数：1
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