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Identification of Mutations in the Thyroxine-Binding Globulin (TBG) Gene in Patients with TBG Deficiency in Korea |
Jung Heo, Sang-Mi Kim, Hyun Jin Ryu, Hyunju Park, Tae Hyuk Kim, Jae Hoon Chung, Hyung-Doo Park, Sun Wook Kim |
Endocrinol Metab. 2022;37(6):870-878. Published online December 7, 2022 DOI: https://doi.org/10.3803/EnM.2022.1591 |
Identification of Mutations in the Thyroxine-Binding Globulin (TBG) Gene in Patients with TBG Deficiency in Korea Two novel mutations in the gene encoding thyroxine-binding globulin (TBG) as a cause of complete TBG deficiency in Taiwan Identification of a novel mutation in thyroxine-binding globulin (TBG) gene associated with TBG-deficiency and its effect on the thyroid function Complete thyroxine-binding globulin (TBG) deficiency caused by a single nucleotide deletion in the TBG gene Partial thyroxine-binding globulin (TBG) deficiency in a family with no detectable mutation of the TBG gene Sequence of the variant thyroxine-binding globulin (TBG) in a Montreal family with partial TBG deficiency Complete Deficiency of Thyroxine-Binding Globulin (TBG-CD Buffalo) Caused by a New Nonsense Mutation in the Thyroxine-Binding Globulin Gene Letter: Free thyroxine index vs. free thyroxine concentration in inherited partial thyroxine binding globulin (TBG) deficiency. Human thyroxine binding globulin (TBG) promoter directs efficient and sustaining transgene expression in liver-specific pattern A Novel Mutation in the TBG Gene Producing Partial Thyroxine-Binding Globulin Deficiency (Glencoe) Identified in 2 Families |