A Novel CYP21A2 Mutation Identified a Patient with Classical 21-Hydroxylase Deficiency

被引：0
|
作者：
Michelato, Dd P. [1 ]
Petroli, R. J. [2 ]
Santos, L. Gd [1 ]
Monlleo, I. L. [2 ]
Mello, M. Pd [1 ]
机构：
[1] Univ Estadual Campinas, UNICAMP, CBMEG, Campinas, SP, Brazil
[2] Univ Fed Alagoas UFAL, Fac Med, Maceio, Brazil
来源：
HORMONE RESEARCH IN PAEDIATRICS | 2016年 / 86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：
P-100
引用
收藏
页码：75 / 75
页数：1
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