Neves, S. C., Mezalira, P. R., Dias, V. M. A., Chagas, A. J., Viana, M., Targovnik, H. M., . . . Rubio, I. G. S. (2010). Monoallelic thyroid peroxidase gene mutation in a patient with congenital hypothyroidism with total iodide organification defect. Web
Citación estilo ChicagoNeves, Solange Caires, Paola Rossi Mezalira, Vera M. A. Dias, Antonio J. Chagas, Maria Viana, Hector Manuel Targovnik, Meyer Knobel, Geraldo Medeiros Neto, and Ileana G. S. Rubio. Monoallelic Thyroid Peroxidase Gene Mutation in a Patient With Congenital Hypothyroidism With Total Iodide Organification Defect. 2010.
Cita MLANeves, Solange Caires, et al. Monoallelic Thyroid Peroxidase Gene Mutation in a Patient With Congenital Hypothyroidism With Total Iodide Organification Defect. 2010.