Molecular Analysis of Congenital Hypothyroidism in Saudi Arabia: SLC26A7 Mutation Is a Novel Defect in Thyroid Dyshormonogenesis

M. Zou,A. Alzahrani,A. Al-Odaib,Mohammad A. Alqahtani,Omer Babiker,Roua A. Al-Rijjal,Huda A. BinEssa,Walaa E. Kattan,Anwar F Al-Enezi,A. A. Al Qarni,Manar Al-faham,E. Baitei,A. Alsagheir,B. Meyer,Yufei Shi

Published 2018 in Journal of Clinical Endocrinology and Metabolism

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