Clinical features and an atypical WT1 mutant site in a child with incomplete Denys-Drash syndrome

Asian J Androl. 2014 Jul-Aug;16(4):647-9. doi: 10.4103/1008-682X.125396.
No abstract available

Publication types

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

MeSH terms

  • Child
  • Denys-Drash Syndrome / diagnosis*
  • Denys-Drash Syndrome / genetics
  • Humans
  • Male
  • Mutation
  • WT1 Proteins / genetics*

Substances

  • WT1 Proteins
  • WT1 protein, human