Identification and functional analysis of novel dual oxidase 2 (DUOX2) mutations in children with congenital or subclinical hypothyroidism (Q24302088)

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Identification and functional analysis of novel dual oxidase 2 (DUOX2) mutations in children with congenital or subclinical hypothyroidism
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    Identification and functional analysis of novel dual oxidase 2 (DUOX2) mutations in children with congenital or subclinical hypothyroidism (English)
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    Giuseppina De Marco
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    Patrizia Agretti
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    Lucia Montanelli
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    Caterina Di Cosmo
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    Brunella Bagattini
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    Melissa De Servi
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    Eleonora Ferrarini
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    Antonio Dimida
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    Andrea Claudia Freitas Ferreira
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    Angelo Molinaro
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    Claudia Ceccarelli
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    Federica Brozzi
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    Aldo Pinchera
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    Paolo Vitti
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    Massimo Tonacchera
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    August 2011
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    96
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    8
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    E1335-9
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