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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Detaylı Bibliyografya
Yayımlandı:Ann Saudi Med
Asıl Yazarlar: Kari, Jameela A., El-Desoky, Sherif M., Gari, Mamdooh, Malik, Khalid, Vega-Warner, Virginia, Lovric, Svjetlana, Bockenhauer, Detlef
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: King Faisal Specialist Hospital and Research Centre 2013
Konular:
Original Article
Online Erişim: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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