Aycan, Z., Cangul, H., Muzza, M., Bas, V., Fugazzola, L., Chatterjee, V., Persani, L. & Schoenmakers, N. (2017) Digenic DUOX1 and DUOX2 Mutations in Cases With Congenital Hypothyroidism. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , 102(9), 3085-3090.