Two novel mutations in the gene encoding thyroxine-binding globulin (TBG) as a cause of complete TBG deficiency in Taiwan-Reference-Cited by-同舟云学术

Two novel mutations in the gene encoding thyroxine-binding globulin (TBG) as a cause of complete TBG deficiency in Taiwan

Published:2003-03-18 Issue:4 Volume:58 Page:409-414
ISSN:0300-0664
Container-title:Clinical Endocrinology
language:en
Short-container-title:

Author:

Su Ching-Chieh,Wu Yi-Chi,Chiu Chih-Yang,Won Justin Ging-Shing,Jap Tjin-Shing

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Endocrinology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2265.2003.01730.x/fullpdf

Reference31 articles.

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2. Thyroxine binding to members and non members of the serine protease inhibitor family;Benvenga;Journal of Endocrinological Investigation,2002

3. Hereditary abnormalities of thyroxine-binding globulin concentration;Burr;Quarterly Journal of Medicine,1980

4. Complete thyroxine- binding globulin deficiency produced by a mutation in acceptor splice site causing frameshift and early termination of translation (TBG-Kankakee);Carvalho;Journal of Clinical Endocrinology and Metabolism,1998a

5. Complete deficiency of thyroxine-binding globulin caused by a new nonsense mutation in the thyroxine-binding globulin gene;Carvalho;Thyroid,1998b

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2. Identification of Mutations in the Thyroxine-Binding Globulin (TBG) Gene in Patients with TBG Deficiency in Korea;Endocrinology and Metabolism;2022-12-31

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