A novel SLC12A3 gene homozygous mutation of Gitelman syndrome in an Asian pedigree and literature review

被引:0
|
作者
Q. Lü
Y. Zhang
C. Song
Z. An
S. Wei
J. Huang
L. Huang
L. Tang
N. Tong
机构
[1] West China Hospital of Sichuan University,Department of Endocrinology and Metabolism
[2] Sichuan University,West China School of Medicine
来源
Journal of Endocrinological Investigation | 2016年 / 39卷
关键词
SLC12A3 gene; Homozygous mutation; Gitelman Syndrome; Pedigree;
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
页码:333 / 340
页数:7
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