IDENTIFICATION OF TWO NOVELS SINGLE NUCLEOTIDE VARIANTS OF THE COMPLEMENT GENES IN A PATIENT WITH THE ASSOCIATION OF PREGNANCY ATYPICAL HEMOLYTIC UREMIC SYNDROME AND C3 GLOMERULOPATHY

被引：0
|
作者：
Greloni, Gustavo [1 ]
Varela, Federico [1 ]
Bratti, Griselda [1 ]
Rosa Diez, Guillermo [1 ]
Dos Santos, Celia [2 ]
Sanchez Luceros, Analia [2 ]
机构：
[1] Hosp Italiano Buenos Aires, Nephrol, Buenos Aires, DF, Argentina
[2] Acad Nacl Med Buenos Aires, Hemathol, Buenos Aires, DF, Argentina
来源：
NEPHROLOGY DIALYSIS TRANSPLANTATION | 2020年 / 35卷
关键词：
D O I：
暂无
中图分类号：
R3 [基础医学]; R4 [临床医学];
学科分类号：
1001 ; 1002 ; 100602 ;
摘要：
P0097
引用
收藏
页码：394 / 394
页数：1
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