A novel mutation in the CYP11B1 gene in a patient with 11β-hydroxylase deficiency

被引：0
|
作者：
Motaghedi, R
Slowinska, B
Cerami, B
Cabrera, M
New, MI
Wilson, RC
机构：
[1] New York Presbyterian Cornell Med Ctr, New York, NY USA
[2] Cornell Univ, Weill Med Coll, New York, NY USA
来源：
AMERICAN JOURNAL OF HYPERTENSION | 2004年 / 17卷 / 05期
关键词：
hypertension; 11 hydroxylase congenital adrenal hyperplasia; genetic-novel mutation;
D O I：
暂无
中图分类号：
R6 [外科学];
学科分类号：
1002 ; 100210 ;
摘要：
P128
引用
收藏
页码：79A / 79A
页数：1
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