Lack of cardiac anomalies in children with NPHS2 mutations

Nephrol Dial Transplant. 2007 May;22(5):1477-9. doi: 10.1093/ndt/gfl833. Epub 2007 Jan 11.
No abstract available

Publication types

  • Letter

MeSH terms

  • Child
  • Child, Preschool
  • Cohort Studies
  • Echocardiography
  • Female
  • Heart Defects, Congenital / genetics*
  • Humans
  • Infant
  • Intracellular Signaling Peptides and Proteins / genetics*
  • Male
  • Membrane Proteins / genetics*
  • Mutation / genetics*
  • Nephrotic Syndrome / genetics
  • Retrospective Studies

Substances

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