Gene Screening of 23 Japanese Families with Complete Thyroxine-Binding Globulin Deficiency: Identification of a Nucleotide Deletion at Codon 352 as a Common Cause.-Reference-Cited by-同舟云学术

Gene Screening of 23 Japanese Families with Complete Thyroxine-Binding Globulin Deficiency: Identification of a Nucleotide Deletion at Codon 352 as a Common Cause.

Published:1993 Issue:5 Volume:40 Page:563-569
ISSN:0918-8959
Container-title:Endocrine Journal
language:en
Short-container-title:Endocr J

Author:

YAMAMORI IKUO¹,MORI YUICHI¹,MIURA YOSHITAKA¹,TANI YOSHIYUKI¹,IMAMURA SHUJI¹,OISO YUTAKA¹,SEO HISAO²

Affiliation:

1. The First Department of Internal Medicine, Nagoya University School of Medicine

2. Department of Endocrinology and Metabolism, Research Institute of Environmental Medicine, Nagoya University

Publisher

Japan Endocrine Society

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

http://www.jstage.jst.go.jp/article/endocrj1993/40/5/40_5_563/_pdf

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