The clinical and molecular characterization of patients with dyshormonogenic congenital hypothyroidism reveals specific diagnostic clues for DUOX2 defects

M. Muzza, S. Rabbiosi, M. C. Vigone, I. Zamproni, V. Cirello, M. A. Maffini, K. Maruca, N. Schoenmakers, L. Beccaria, F. Gallo, S. M. Park, P. Beck-Peccoz, L. Persani, G. Weber, L. Fugazzola

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