The clinical and molecular characterization of patients with dyshormonogenic congenital hypothyroidism reveals specific diagnostic clues for DUOX2 defects - Muzza, M; Rabbiosi, S; Vigone, M C; Zamproni, I; Cirello, V; Maffini, M A; Maruca, K; Schoenmakers, N; Beccaria, L; Gallo, F; Park, S M; Beck-Peccoz, P; Persani, L; Weber, G; Fugazzola, L (J Clin Endocrinol Metab, 2014)