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. 2017 Jun 16;102(9):3085–3090. doi: 10.1210/jc.2017-00529

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Figure 1. — Pedigree diagram summarizing clinical phenotype and genotype. Black: homozygotes for the DUOX2 and DUOX1 mutations; central black dot: heterozygotes for the two mutations. The degree of iodine deficiency on the spot urinary measurement is classified according to World Health Organization criteria. DUOX1 fs, DUOX1 p.Val607Aspfs*43; het, heterozygous; hom, homozygous.