A novel mutation causing complete deficiency of thyroxine binding globulin-Reference-Cited by-同舟云学术

A novel mutation causing complete deficiency of thyroxine binding globulin

Published:1997-07 Issue:1 Volume:47 Page:1-5
ISSN:0300-0664
Container-title:Clinical Endocrinology
language:en
Short-container-title:Clinical Endocrinology

Author:

Ueta Yoshihiko¹,Mitani Yasuo¹,Yoshida Akio¹,Taniguchi Shinichi¹,Mori Atsumi¹,Hattori Kimihiko¹,Hisatome Ichiro¹,Manabe Ichiro¹,Takeda Kyoko²,Sato Ryoichi³,Ahmmed Gias U.¹,Tsuboi Mariko¹,Ohtahara Akira¹,Hiroe Koh¹,Tanaka Yasushi¹,Shigemasa Chiaki¹

Affiliation:

1. First Department of Internal Medicine, Tottori University, Faculty of Medicine, Yonago,

2. Second Department of internal Medicine, Kochi Medical School, Kochi,

3. First Department of Internal Medicine, Kinki University School of Medicine, Osaka, Japan

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Endocrinology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1046/j.1365-2265.1997.2181030.x

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1. 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

2. Rare thyroid non-neoplastic diseases;Thyroid Research;2015-04-11

3. Two Novel Mutations in the Serpina7 Gene Are Associated with Complete Deficiency of Thyroxine-Binding Globulin;European Thyroid Journal;2015

4. A Novel Mutation (del 1711 G) in theTBGGene as a Cause of Complete TBG Deficiency;Thyroid;2007-11

5. TGB Deficiency: description of two novel mutations associated with complete TBG deficiency and review of the literature;Journal of Molecular Medicine;2006-09-01