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Nonautoimmune congenital hyperthyroidism due to p.Asp633Glu mutation in the TSHR gene | |
Won Kyoung Cho, Moon-Bae Ahn, Woori Jang, Hyojin Chae, Myungshin Kim, Byung-Kyu Suh | |
Ann Pediatr Endocrinol Metab. 2018;23(4):235-239. Published online December 31, 2018 DOI: https://doi.org/10.6065/apem.2018.23.4.235 |
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Nonautoimmune congenital hyperthyroidism due to p.Asp633Glu mutation in the TSHR gene Subclinical hyperthyroidism due to a thyrotropin receptor (TSHR) gene mutation (S505R) MON-264 Familial Neonatal Nonautoimmune Hyperthyroidism Due To A Thyrotropin Receptor Gene Mutation (A619G). Sporadic Nonautoimmune Congenital Hyperthyroidism due to a Strong Activating Mutation of the Thyrotropin Receptor Gene Congenital Nonautoimmune Hyperthyroidism in a Nonidentical Twin Caused by a Sporadic Germline Mutation in the Thyrotropin Receptor Gene MON-265 Congenital Hypothyroidism and Bilateral Ptosis Due to a Novel TSHR Gene Mutation Long-Term Carbimazole Treatment of Neonatal Nonautoimmune Hyperthyroidism due to a New Activating TSH Receptor Gene Mutation (Ala428Val) Sporadic congenital nonautoimmune hyperthyroidism caused by P639S mutation in thyrotropin receptor gene Premature birth and low birth weight associated with nonautoimmune hyperthyroidism due to an activating thyrotropin receptor gene mutation A Japanese family with nonautoimmune hyperthyroidism caused by a novel heterozygous thyrotropin receptor gene mutation |