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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Detalhes bibliográficos
Publicado no:Ann Saudi Med
Main Authors: Kari, Jameela A., El-Desoky, Sherif M., Gari, Mamdooh, Malik, Khalid, Vega-Warner, Virginia, Lovric, Svjetlana, Bockenhauer, Detlef
Formato: Artigo
Idioma:Inglês
Publicado em: King Faisal Specialist Hospital and Research Centre 2013
Assuntos:
Original Article
Acesso em linha: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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