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| Persistent goiter with congenital hypothyroidism due to mutation in DUOXA2 gene | |
| So Yoon Jung, Jeongho Lee, Dong Hwan Lee | |
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Ann Pediatr Endocrinol Metab. 2020;25(1):57-62. Published online March 31, 2020 DOI: https://doi.org/10.6065/apem.2020.25.1.57 |
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Persistent goiter with congenital hypothyroidism due to mutation in DUOXA2 gene Annals of Pediatric Endocrinology & Metabolism. 2020;25(1):57-62  Dyshormonogenetic goiter-like changes in a child with congenital hypothyroidism and a euthyroid adult Diagnostic Cytopathology. 2012;41(8):720-724 MON-265 Congenital Hypothyroidism and Bilateral Ptosis Due to a Novel TSHR Gene Mutation Journal of the Endocrine Society. 2019;3(Supplement_1): Congenital Goiter with Hypothyroidism Caused by a 5′ Splice Site Mutation in the Thyroglobulin Gene Thyroid. 2001;11(7):685-690 Respiratory insufficiency in a newborn with congenital hypothyroidism due to a new mutation of TTF-1/NKX2.1 gene Pediatric Pulmonology. 2013;49(3):E42-E44 Mutation Screening of DUOX2 Gene in Children with Congenital Hypothyroidism . 2020; Congenital hypothyroidism due to thyroglobulin deficiency: a case report with a novel mutation in TG gene Annals of Pediatric Endocrinology & Metabolism. 2019;24(3):199-202 Clinical and Genetic Analysis of a Compound Heterozygous Mutation in the Thyroglobulin Gene in a Chinese Twin Family With Congenital Goiter and Hypothyroidism Twin Research and Human Genetics. 2012;15(1):126-132 Congenital dyshormonogenic hypothyroidism with goiter caused by a sodium/iodide symporter (SLC5A5) mutation in a family of Shih-Tzu dogs Domestic Animal Endocrinology. 2018;65:1-8 Genetics and phenomics of hypothyroidism and goiter due to iodotyrosine deiodinase (DEHAL1) gene mutations Molecular and Cellular Endocrinology. 2010;322(1-2):91-98 |
