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Le mutazioni di DUOX2/DUOXA2 causano frequentemente un ipotiroidismo congenito che sfugge all’identificazione nello screening neonatale nel Regno Unito

  • NOVITÀ IN ENDOCRINOLOGIA
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Bibliografia

  1. Muzza M, Fugazzola L (2017) Disorders of H2O2 generation. Best Pract Res Clin Endocrinol Metab 31:225–240

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  2. Muzza M, Rabbiosi S, Vigone MC et al. (2014) The clinical and molecular characterization of patients with dyshormonogenic congenital hypothyroidism reveals specific diagnostic clues for DUOX2 defects. J Clin Endocrinol Metab 99:E544–E553

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Authors and Affiliations

  1. Dipartimento di Fisiopatologia Medico Chirurgica e dei Trapianti, Centro Tiroide Auxologico, Istituto Auxologico Italiano IRCCS, Università di Milano, Milano, Italia

    Laura Fugazzola

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  1. Laura Fugazzola
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Correspondence to Laura Fugazzola.

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Fugazzola, L. Le mutazioni di DUOX2/DUOXA2 causano frequentemente un ipotiroidismo congenito che sfugge all’identificazione nello screening neonatale nel Regno Unito. L'Endocrinologo 20, 309–310 (2019). https://doi.org/10.1007/s40619-019-00626-w

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  • DOI: https://doi.org/10.1007/s40619-019-00626-w

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