Novel frameshift mutation causes early termination of the thyroxine-binding globulin protein and complete thyroxine-binding globulin deficiency in a Chinese family: A case report

Author:

Dang Ping-Ping,Xiao Wei-Wei,Shan Zhong-Yan,Xi Yue,Wang Ran-Ran,Yu Xiao-Hui,Teng Wei-Ping,Teng Xiao-Chun

Publisher

Baishideng Publishing Group Inc.

Subject

General Medicine

Reference30 articles.

1. Inherited Thyroxine-Binding Globulin Abnormalities in Man*

2. Refetoff S. Thyroid Hormone Serum Transport Proteins. In: Feingold KR, Anawalt B, Boyce A, editors. Endotext. South Dartmouth: MDText.com, Inc., 2000

3. Robbins J, Rall JE. Zone electrophoresis in filter paper of serum I 131 after radioiodide administration. Proc Soc Exp Biol Med 1952; 81: 530-536

4. Trent JM, Flink IL, Morkin E, van Tuinen P, Ledbetter DH. Localization of the human thyroxine-binding globulin gene to the long arm of the X chromosome (Xq21-22). Am J Hum Genet 1987; 41: 428-435

5. Mori Y, Miura Y, Oiso Y, Hisao S, Takazumi K. Precise localization of the human thyroxine-binding globulin gene to chromosome Xq22.2 by fluorescence in situ hybridization. Hum Genet 1995; 96: 481-482

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