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Two compound heterozygous mutations (c.215delA/c.2422T→C and c.387delC/c.1159G→A) in the thyroid peroxidase gene responsible for congenital goitre and iodide organification defect
Carina M. Rivolta, Mariana Louis-Tisserand, Viviana Varela, Laura Gruñeiro-Papendieck, Ana Chiesa, Rogelio González-Sarmiento, Héctor M. TargovnikVolume:
67
Year:
2007
Language:
english
Pages:
9
DOI:
10.1111/j.1365-2265.2007.02869.x
File:
PDF, 1.44 MB
english, 2007