Can inactivation mutation in the thyroid stimulating hormone receptor gene and hyperthyroidism coexist?: A case report

We found the G132R heterozygous mutation of thyroid stimulating hormone receptor (TSHR) gene in a patient with recurrent hypokalemia. Because the patient had a medical history of hyperthyroidism, the mutation was suspected to be related to hyperthyroidism at first. Subsequently, the expression and f...

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Veröffentlicht in:	Medicine (Baltimore) 2024-01, Vol.103 (3), p.e36950-e36950
Hauptverfasser:	Liu, Yanfang, Li, Jie, Gao, Fei, Zhao, Changjian, Yang, Luyang, Liu, Yunfeng
Format:	Artikel
Sprache:	eng
Schlagworte:	Female Humans Hyperthyroidism - genetics Hypothyroidism - complications Mutation Receptors, G-Protein-Coupled - genetics Receptors, Thyrotropin - genetics RNA, Messenger
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