Monoallelic thyroid peroxidase gene mutation in a patient...

Arquivos Brasileiros de Endocrinologia & Metabologia 2010 / 11 Vol. 54; Iss. 8

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.
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Volume:
54
Journal:
Arquivos Brasileiros de Endocrinologia & Metabologia
DOI:
10.1590/S0004-27302010000800012
Date:
November, 2010
File:
PDF, 1.08 MB
2010
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