Gene mutation analysis in 12 Chinese children with congenital nephrotic syndrome

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 the gene...

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Detalles Bibliográficos
Autores principales: Li, Guo-min, Cao, Qi, Shen, Qian, Sun, Li, Zhai, Yi-hui, Liu, Hai-mei, An, Yu, Xu, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6311020/
https://www.ncbi.nlm.nih.gov/pubmed/30594156
http://dx.doi.org/10.1186/s12882-018-1184-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6311020/
https://www.ncbi.nlm.nih.gov/pubmed/30594156
http://dx.doi.org/10.1186/s12882-018-1184-y

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