Gene mutation analysis in 12 Chinese children with congenital nephrotic syndrome

Gene mutation analysis in 12 Chinese children with congenital nephrotic syndrome

Abstract Background Congenital nephrotic syndrome (CNS) is characterised by increased proteinuria, hypoproteinemia, and edema beginning in the first 3 months of life. Recently, molecular genetic studies have identified several genes involved in the pathogenesis of CNS. A systematic investigation of...

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Bibliographic Details
Main Authors: Guo-min Li, Qi Cao, Qian Shen, Li Sun, Yi-hui Zhai, Hai-mei Liu, Yu An, Hong Xu
Format: Article
Language:English
Published: BMC 2018-12-01
Series:BMC Nephrology
Subjects:
Chinese children
Congenital nephritic syndrome
NPHS1 gene
WT1 gene
COQ6 gene
Online Access:http://link.springer.com/article/10.1186/s12882-018-1184-y

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http://link.springer.com/article/10.1186/s12882-018-1184-y

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