1. A truncating TPO mutation (Y55X) in patients with hypothyroidism and total iodide organification defect. (August 2015) Authors: Cangul, Hakan; Darendeliler, Feyza; Saglam, Yaman; Kucukemre, Banu; Kendall, Michaela; Boelaert, Kristien; Barrett, Timothy G.; Maher, Eamonn R. Journal: Endocrine research Issue: Volume 40:Number 3(2015:Aug.) Page Start: 146 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Thyroid dyshormonogenesis is mainly caused by TPO mutations in consanguineous community. (6th May 2013) Authors: Cangul, Hakan; Aycan, Zehra; Olivera‐Nappa, Alvaro; Saglam, Halil; Schoenmakers, Nadia A.; Boelaert, Kristien; Cetinkaya, Semra; Tarim, Omer; Bober, Ece; Darendeliler, Feyza; Bas, Veysel; Demir, Korcan; Aydin, Banu K.; Kendall, Michaela; Cole, Trevor; Högler, Wolfgang; Chatterjee, V. Krishna K.; ... Journal: Clinical endocrinology Issue: Volume 79:Number 2(2013:Aug.) Page Start: 275 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗