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Foxd2 Dysfunction is Implicated in Syndromic Congenital Anomalies of the Kidney and Urinary Tract (cakut)

  • FOXD2 Res Consortium
  • Technical University of Munich
  • Dept Human Genet
  • Hacettepe University
  • Max Delbrück Center for Molecular Medicine in the Helmholtz Association
  • University of Freiburg
  • Istanbul University - Cerrahpasa

Research output: Contribution to journalMeeting Abstractpeer-review

Original languageEnglish
Pages (from-to)S128-S129
Number of pages2
JournalPediatric Nephrology
Volume38
Publication statusPublished - Sept 2023

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