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A truncating TPO mutation (Y55X) in patients with hypothyroidism and total iodide organification defect

  • Hakan Cangul*
  • , Feyza Darendeliler
  • , Yaman Saglam
  • , Banu Kucukemre
  • , Michaela Kendall
  • , Kristien Boelaert
  • , Timothy G. Barrett
  • , Eamonn R. Maher
  • *Corresponding author for this work
  • Bahcesehir University School of Medicine
  • Istanbul University
  • Medical Park Goztepe Hospital
  • University of Southampton, Faculty of Medicine
  • University College Birmingham

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Biochemistry, Genetics and Molecular Biology