A Novel Mutation Causing Complete Thyroxine-Binding Globulin Deficiency (TBG-CD-Negev) among the Bedouins in Southern Israel-Reference-Cited by-同舟云学术

A Novel Mutation Causing Complete Thyroxine-Binding Globulin Deficiency (TBG-CD-Negev) among the Bedouins in Southern Israel

Published:2000-10-01 Issue:10 Volume:85 Page:3687-3689
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:

Author:

Miura Yoshitaka¹,Hershkovitz Eli²,Inagaki Akemi¹,Parvari Ruti³,Oiso Yutaka¹,Phillip Moshe²

Affiliation:

1. First Department of Internal Medicine, Nagoya University School of Medicine (Y.M., A.I., Y.O.), Nagoya, Japan

2. Department of Pediatrics (E.H., M.P.), Beer Sheva 84101, Israel

3. Laboratory of Molecular Genetics (R.P.), Soroka Medical Center, Faculty of Health Sciences, Ben Gurion University of the Negev, Beer Sheva 84101, Israel

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Link

http://academic.oup.com/jcem/article-pdf/85/10/3687/10402993/jcem3687.pdf

Reference22 articles.

1. Inherited thyroxine-binding globulin abnormalities in man.;Endocr Rev,1989

2. Implications of the three-dimensional structure of alpha 1-antitrypsin for structure and function of serpins.;Huber;Biochemistry,1989

3. Human thyroxine-binding globulin gene: complete sequence and transcriptional regulation.;Hayashi;Mol Endocrinol,1993

4. Radioimmunoassays specific for the tertiary and primary structures of thyroxine-binding globulin (TBG): measurement of denatured TBG in serum.;Refetoff;J Clin Endocrinol Metab,1984

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