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Monoallelic thyroid peroxidase gene mutation in a patient with congenital hypothyroidism with total iodide organification defectNeves, Solange Caires ; Mezalira, Paola Rossi ; Dias, Vera M A ; Chagas, Antonio J ; Viana, Maria ; Targovnik, Hector ; Knobel, Meyer ; Medeiros-Neto, Geraldo ; Rubio, Ileana G SArquivos brasileiros de endocrinologia e metabologia, 2010-11, Vol.54 (8), p.732-737Brazil: Sociedade Brasileira de Endocrinologia e MetabologiaTexto completo disponível |