A truncating DUOX2 mutation (R434X) causes severe congenital hypothyroidism
- Hakan Cangul*
- , Zehra Aycan
- , Michaela Kendall
- , Veysel N. Bas
- , Yaman Saglam
- , Timothy G. Barrett
- , Eamonn R. Maher
*Corresponding author for this work
- Bahcesehir University School of Medicine
- Children Research Hospital
- University of Southampton, Faculty of Medicine
- Medical Park Goztepe Hospital
- University College Birmingham
Research output: Contribution to journal › Article › peer-review
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