Familial nephrotic syndrome caused by COQ2 mutations, an inherited mitochondriopathy

被引：0
|
作者：
Voskanyan, Milena [1 ,2 ]
Sarinyan, Sofi [1 ,2 ]
Gaspert, Ariana [3 ]
Bergmann, Carsten [4 ,5 ]
Weber, Stefanie [6 ]
Leumann, Ernst [7 ]
Sarkissian, Ashot [1 ,2 ]
机构：
[1] Arabkir Med Ctr, Nephrol Dept, Yerevan, Armenia
[2] Yerevan State Med Univ, Yerevan, Armenia
[3] Univ Hosp Zurich, Inst Pathol & Mol Pathol, Zurich, Switzerland
[4] Bioscientia, Ctr Human Genet, Ingelheim, Germany
[5] Univ Freiburg, Dept Nephrol, Freiburg, Germany
[6] Philipps Univ Marburg, Univ Childrens Hosp, Marburg, Germany
[7] Univ Childrens Hosp, Zurich, Switzerland
来源：
SWISS MEDICAL WEEKLY | 2016年 / 146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 4
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收藏
页码：5S / 5S
页数：1
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