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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Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4589073/
https://www.ncbi.nlm.nih.gov/pubmed/26420286
http://dx.doi.org/10.1186/s12881-015-0231-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4589073/
https://www.ncbi.nlm.nih.gov/pubmed/26420286
http://dx.doi.org/10.1186/s12881-015-0231-9

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