Monoallelic thyroid peroxidase gene mutation in a patient with congenital hypothyroidism with total iodide organification defect
Solange Caires Neves Paola Rossi Mezalira; Vera M. A Dias; Antonio J Chagas; Maria Viana; Hector Targovnik; Meyer Knobel; Geraldo Medeiros-Neto; Ileana G. S Rubio
Arquivos Brasileiros de Endocrinologia e Metabologia São Paulo v. 54, n. 8, p. 732-737, 2010São Paulo 2010
Available at FM - Fac. Medicina (BCSEP 343 2010 )(GetIt)