Author:
Agretti Patrizia,Bagattini Brunella,De Marco Giuseppina,Di Cosmo Caterina,Dionigi Gianlorenzo,Vitti Paolo,Tonacchera Massimo
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Reference7 articles.
1. G. Ford, S.H. LaFranchi, Screening for congenital hypothyroidism: a worldwide view of strategies. Best. Pract. Res. Clin. Endocrinol. Metab. 28(2), 175–187 (2014)
2. H. Grasberger, S. Refetoff, Genetic causes of congenital hypothyroidism due to dyshormonogenesis. Curr. Opin. Pediatr. 23(4), 421–428 (2011)
3. S. Kosugi, Y. Sato, A. Matsuda, Y. Ohyama, K. Fujieda, H. Inomata, T. Kameya, O. Isozaki, S.M. Jhiang, High prevalence of T354P sodium/iodide symporter mutation in Japanese patients with iodide transport defect who have heterogeneous clinical pictures. J. Clin. Endocrinol. Metab. 83(11), 4123–4129 (1998)
4. J.B. Stanbury, E.M. Chapman, Congenital hypothyroidism with goiter. Absence of an iodide-concentrating mechanism. Lancet. 1(7135), 1162–1165 (1960)
5. C. Spitzweg, J.C. Morris, Genetics and phenomics of hypothyroidism and goiter due to SLC24A4 mutations. Mol. Cell. Endocrinol. 322(1–2), 56–63 (2010)
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