Expanding the Clinical Spectrum of Congenital Nephrotic Syndrome Caused by NPHS1 Mutations

Nephrol Dial Transplant. 2010 Sep;25(9):2837-9. doi: 10.1093/ndt/gfq434. Epub 2010 Jul 21.

MeSH terms

  • Genotype
  • Humans
  • Membrane Proteins / genetics*
  • Mutation / genetics*
  • Nephrotic Syndrome / congenital*
  • Nephrotic Syndrome / genetics*
  • Nephrotic Syndrome / pathology
  • Phenotype

Substances

  • Membrane Proteins
  • nephrin