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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
Annals of Pediatric Endocrinology & Metabolism. 2018;23(4):235-239   Crossref logo
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MON-264 Familial Neonatal Nonautoimmune Hyperthyroidism Due To A Thyrotropin Receptor Gene Mutation (A619G).
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Subclinical hyperthyroidism due to a thyrotropin receptor (TSHR) gene mutation (S505R)
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Sporadic Nonautoimmune Congenital Hyperthyroidism due to a Strong Activating Mutation of the Thyrotropin Receptor Gene
Thyroid. 2000;10(10):859-863   Crossref logo
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MON-265 Congenital Hypothyroidism and Bilateral Ptosis Due to a Novel TSHR Gene Mutation
Journal of the Endocrine Society. 2019;3(Supplement_1):   Crossref logo
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A Japanese family with nonautoimmune hyperthyroidism caused by a novel heterozygous thyrotropin receptor gene mutation
Pediatric Research. 2014;75(6):749-753   Crossref logo
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Congenital Nonautoimmune Hyperthyroidism in a Nonidentical Twin Caused by a Sporadic Germline Mutation in the Thyrotropin Receptor Gene
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Sporadic congenital nonautoimmune hyperthyroidism caused by P639S mutation in thyrotropin receptor gene
European Journal of Pediatrics. 2012;171(7):1133-1137   Crossref logo
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Long-Term Carbimazole Treatment of Neonatal Nonautoimmune Hyperthyroidism due to a New Activating TSH Receptor Gene Mutation (Ala428Val)
Hormone Research in Paediatrics. 2005;64(4):203-208   Crossref logo
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Premature birth and low birth weight associated with nonautoimmune hyperthyroidism due to an activating thyrotropin receptor gene mutation
Clinical Endocrinology. 2004;60(6):711-718   Crossref logo
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