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Monoallelic thyroid peroxidase gene mutation in a patient with congenital hypothyroidism with total iodide organification defect
Author(s):
SC Neves
,
PR Mezalira
,
VM Dias
,
AJ Chagas
,
M. Viana
,
HM Targovnik
Publication date:
2010
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Bioscientifica Open Endocrinology
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ScienceOpen disciplines:
Endocrinology & Diabetes
,
Medicine
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