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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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| Publié dans: | BMC Med Genet |
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| Auteurs principaux: | , , , , , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
BioMed Central
2015
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| Sujets: | |
| Accès en ligne: | 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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