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Clin Chim Acta 458: 30\u201334.","DOI":"10.1016\/j.cca.2016.04.019"},{"key":"9","doi-asserted-by":"crossref","unstructured":"9 Tan M, Huang Y, Jiang X, Li P, Tang C, et al. (2016) The prevalence, clinical, and molecular characteristics of congenital hypothyroidism caused by DUOX2 mutations: a population-based cohort study in Guangzhou. Horm Metab Res 48: 581\u2013588.","DOI":"10.1055\/s-0042-112224"},{"key":"10","doi-asserted-by":"crossref","unstructured":"10 Maruo Y, Takahashi H, Soeda I, Nishikura N, Matsui K, et al. (2008) Transient congenital hypothyroidism caused by biallelic mutations of the dual oxidase 2 gene in Japanese patients detected by a neonatal screening program. J Clin Endocrinol Metab 93: 4261\u20134267.","DOI":"10.1210\/jc.2008-0856"},{"key":"11","doi-asserted-by":"crossref","unstructured":"11 Maruo Y, Nagasaki K, Matsui K, Mimura Y, Mori A, et al. (2016) Natural course of congenital hypothyroidism by dual oxidase 2 mutations from the neonatal period through puberty. Eur J Endocrinol 174: 453\u2013463.","DOI":"10.1530\/EJE-15-0959"},{"key":"12","doi-asserted-by":"crossref","unstructured":"12 Chow YP, Abdul Murad NA, Mohd Rani Z, Khoo JS, Chong PS, et al. (2017) Exome sequencing identifies SLC26A4, GJB2, SCARB2 and DUOX2 mutations in 2 siblings with Pendred syndrome in a Malaysian family. Orphanet J Rare Dis 12: 40.","DOI":"10.1186\/s13023-017-0575-7"},{"key":"13","unstructured":"13 Belforte FS, Olcese MC, Siffo S, Papendieck P, Enacan R, et al. (2016) Codon mutations (p.F353Pfs*36\/p.Y425X) in DUOX2 gene associated with transient congenital hypothyroidism: report of a family and literature review. Ann Thyroid Res 2: 69\u201378."},{"key":"14","doi-asserted-by":"crossref","unstructured":"14 Park KJ, Park HK, Kim YJ, Lee KR, Park JH, et al. (2016) DUOX2 mutations are frequently associated with congenital hypothyroidism in the Korean population. Ann Lab Med 36: 145\u2013153.","DOI":"10.3343\/alm.2016.36.2.145"},{"key":"15","unstructured":"15 Chai J, Yang XL, Guo MZ, Liu L, Liu SG, et al. (2015) DUOX2 mutations in children with congenital hypothyroidism. Zhongguo Dang Dai Er Ke Za Zhi 17: 40\u201344 (In Chinese)."},{"key":"16","doi-asserted-by":"crossref","unstructured":"16 Jiang H, Wu J, Ke S, Hu Y, Fei A, et al. (2016) High prevalence of DUOX2 gene mutations among children with congenital hypothyroidism in central China. Eur J Med Genet 59: 526\u2013531.","DOI":"10.1016\/j.ejmg.2016.07.004"},{"key":"17","doi-asserted-by":"crossref","unstructured":"17 Zheng X, Ma SG, Qiu YL, Guo ML, Shao XJ (2016) A novel c.554+5C&gt;T mutation in the DUOXA2 gene combined with p.R885Q mutation in the DUOX2 gene causing congenital hypothyroidism. J Clin Res Pediatr Endocrinol 8: 224\u2013227.","DOI":"10.4274\/jcrpe.2380"},{"key":"18","doi-asserted-by":"crossref","unstructured":"18 Narumi S, Muroya K, Asakura Y, Aachi M, Hasegawa T (2011) Molecular basis of thyroid dyshormonogenesis: genetic screening in population-based Japanese patients. J Clin Endocrinol Metab 96: E1838\u2013E1842.","DOI":"10.1210\/jc.2011-1573"},{"key":"19","doi-asserted-by":"crossref","unstructured":"19 Jin HY, Heo SH, Kim YM, Kim GH, Choi JH, et al. (2014) High frequency of DUOX2 mutations in transient or permanent congenital hypothyroidism with eutopic thyroid glands. Horm Res Paediatr 82: 252\u2013260.","DOI":"10.1159\/000362235"},{"key":"20","doi-asserted-by":"crossref","unstructured":"20 Matsuo K, Tanahashi Y, Mukai T, Suzuki S, Tajima T, et al. (2016) High prevalence of DUOX2 mutations in Japanese patients with permanent congenital hypothyroidism or transient hypothyroidism. 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