Heterozygous NPHS1 or NPHS2 mutations in responsive nephrotic syndrome and the multifactorial origin of proteinuria

Kidney Int. 2004 Oct;66(4):1715-6. doi: 10.1111/j.1523-1755.2004.938_9.x.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Heterozygote
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • Membrane Proteins / genetics*
  • Mutation
  • Nephrotic Syndrome / genetics*
  • Proteins / genetics*
  • Proteinuria / genetics*

Substances

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