Monoallelic thyroid peroxidase gene mutation in a patient with congenital hypothyroidism with total iodide organification defect - Neves, Solange Caires; Mezalira, Paola Rossi; Dias, Vera M. A.; Chagas, Antonio J.; Viana, Maria; Targovnik, Hector; Knobel, Meyer; Medeiros-Neto, Geraldo; Rubio, Ileana G. S. (Arquivos Brasileiros de Endocrinologia e Metabologia, 2010)