NPHS2 mutations account for only 15 % of nephrotic syndrome cases

BACKGROUND: Nephrotic syndrome is traditionally classified on the basis of the response to standard steroid treatment. Mutations in more than 24 genes have been associated with nephrotic syndrome in children, although the great majority of steroid-resistant cases have been attributed to mutations in...

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Veröffentlicht in:BMC Med Genet
Hauptverfasser: Guaragna, Mara Sanches, Lutaif, Anna Cristina GB, Piveta, Cristiane SC, Souza, Marcela L., de Souza, Suéllen R., Henriques, Taciane B., Maciel-Guerra, Andréa T., Belangero, Vera MS, Guerra-Junior, Gil, De Mello, Maricilda P.
Format: Artigo
Sprache:Inglês
Veröffentlicht: BioMed Central 2015
Schlagworte:
Research Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4589073/
https://ncbi.nlm.nih.gov/pubmed/26420286
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-015-0231-9
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