Gene screening of thyroxine-binding globulin (TBG) deficiencies in the Japanese: only two mutations account for TBG deficiencies in the Japanese
Author:
Publisher
The Endocrine Society
Subject
Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism
Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. A novel variant in Serpina7 gene in a family with thyroxine-binding globulin deficiency;Endocrine;2009-05-05
2. Two novel mutations in the gene encoding thyroxine-binding globulin (TBG) as a cause of complete TBG deficiency in Taiwan;Clinical Endocrinology;2003-03-18
3. A novel mutation causing complete thyroxine-binding globulin deficiency (TBG-CD-Negev) among the Bedouins in southern Israel;J CLIN ENDOCR METAB;2000
4. Autosomally Transmitted Low Concentration of Thyroxine-Binding Globulin;Thyroid;1999-02
5. Gene Amplification as a Common Cause of Inherited Thyroxine-Binding Globulin Excess. Analysis of One Familial and Two Sporadic Cases.;Endocrine Journal;1999
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