A Novel Mutation (del 1711 G) in theTBGGene as a Cause of Complete TBG Deficiency-Reference-Cited by-同舟云学术

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A Novel Mutation (del 1711 G) in theTBGGene as a Cause of Complete TBG Deficiency

Published:2007-11 Issue:11 Volume:17 Page:1143-1146
ISSN:1050-7256
Container-title:Thyroid
language:en
Short-container-title:Thyroid

Author:

Lacka Katarzyna¹,Nizankowska Teresa²,Ogrodowicz Agnieszka³,Lacki Jan K.⁴

Affiliation:

1. Chair of Endocrinology, University of Medical Sciences, Poznan, Poland.

2. Outpatient Clinic of Endocrine Diseases, Rzeszow, Poland.

3. Outpatient Clinic of Internal Diseases, Poznan, Poland.

4. Department of Connective Tissue Diseases, Institute of Rheumatology, Warsaw, Poland.

Publisher

Mary Ann Liebert Inc

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

https://www.liebertpub.com/doi/pdf/10.1089/thy.2007.0023

Reference20 articles.

1. Thyroxine-Binding Globulin: Organization of the Gene and Variants

2. The Thyroxine-Binding Proteins

3. Precise localization of the human thyroxine-binding globulin gene to chromosome Xq22.2 by fluorescence in situ hybridization

4. Complete amino acid sequence of human thyroxine-binding globulin deduced from cloned DNA: close homology to the serine antiproteases.

5. Inheritance of Decreased Thyroxine-Binding by the Thyroxine-Binding Globulin1

Cited by 8 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. Partial Thyroid Hormone-Binding Globulin Deficiency: A Case Report and Literature Review;Diabetes, Metabolic Syndrome and Obesity;2023-07

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

3. Identification of a novel mutation in thyroxine-binding globulin (TBG) gene associated with TBG-deficiency and its effect on the thyroid function;Journal of Endocrinological Investigation;2021-11-10

4. First report of inherited thyroxine-binding globulin deficiency in Iran caused by a known de novo mutation in SERPINA7;Molecular Genetics and Metabolism Reports;2016-09

5. Common Genetic Variation In Cellular Transport Genes and Epithelial Ovarian Cancer (EOC) Risk;PLOS ONE;2015-06-19

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