Novel NPHS1 gene mutations in a Chinese family with congenital nephrotic syndrome

J Genet. 2016 Mar;95(1):161-6. doi: 10.1007/s12041-015-0598-6.
No abstract available

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • China
  • Female
  • Humans
  • Infant, Newborn
  • Male
  • Membrane Proteins / genetics*
  • Mutation*
  • Nephrotic Syndrome / congenital*
  • Nephrotic Syndrome / genetics
  • Pedigree

Substances

  • Membrane Proteins
  • nephrin