Steroid-resistant nephrotic syndrome: impact of genetic testing

BACKGROUND AND OBJECTIVES: Mutations in several genes are known to cause steroid-resistant nephrotic syndome (SRNS), most commonly in NPHS1, NPHS2, and WT1. Our aims were to determine the frequency of mutations in these genes in children with SRNS, the response of patients with SRNS to various immun...

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Bibliografske podrobnosti
izdano v:Ann Saudi Med
Main Authors: Kari, Jameela A., El-Desoky, Sherif M., Gari, Mamdooh, Malik, Khalid, Vega-Warner, Virginia, Lovric, Svjetlana, Bockenhauer, Detlef
Format: Artigo
Jezik:Inglês
Izdano: King Faisal Specialist Hospital and Research Centre 2013
Teme:
Original Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC6074900/
https://ncbi.nlm.nih.gov/pubmed/24413855
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5144/0256-4947.2013.533
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