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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Detalles Bibliográficos
Autores principales: Kari, Jameela A., El-Desoky, Sherif M., Gari, Mamdooh, Malik, Khalid, Vega-Warner, Virginia, Lovric, Svjetlana, Bockenhauer, Detlef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: King Faisal Specialist Hospital and Research Centre 2013
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6074900/
https://www.ncbi.nlm.nih.gov/pubmed/24413855
http://dx.doi.org/10.5144/0256-4947.2013.533

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6074900/
https://www.ncbi.nlm.nih.gov/pubmed/24413855
http://dx.doi.org/10.5144/0256-4947.2013.533

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