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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Ann Saudi Med
Päätekijät: Kari, Jameela A., El-Desoky, Sherif M., Gari, Mamdooh, Malik, Khalid, Vega-Warner, Virginia, Lovric, Svjetlana, Bockenhauer, Detlef
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: King Faisal Specialist Hospital and Research Centre 2013
Aiheet:
Original Article
Linkit: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
Tagit: Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!

Samankaltaisia teoksia