NPHS2 gene mutation in an Iranian family with familial steroid-resistant nephrotic syndrome

Nefrologia. 2012;32(5):674-6. doi: 10.3265/Nefrologia.pre2012.Jun.11428.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Child
  • Child, Preschool
  • Female
  • Humans
  • Infant
  • Intracellular Signaling Peptides and Proteins / genetics*
  • Iran
  • Male
  • Membrane Proteins / genetics*
  • Mutation
  • Nephrotic Syndrome / congenital*
  • Nephrotic Syndrome / genetics
  • Pedigree

Substances

  • Intracellular Signaling Peptides and Proteins
  • Membrane Proteins
  • NPHS2 protein

Supplementary concepts

  • Nephrotic syndrome, idiopathic, steroid-resistant