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Article

Mass screening for complete deficiency of thyroxine-binding globulin in adult Japanese by comprehensive health examination.

Internal medicine (Tokyo, Japan) - 1 Apr 1996

Noguchi T, Miki T, Takamatsu J, Nakajima T, Kumahara Y

Abstract excerpt

The incidence of complete thyroxine-binding globulin (TBG) deficiency (TBG-CD) was determined for a Japanese population from a comprehensive health examination, in which a T3 resin uptake test of the upper 5% (78 subjects from among 1,589 men) was the screening line for TBG-CD. Further analysis of the known mutation in TBG-CD gene of the Japanese population (reported as TBG-CDJ with codon 352 deletion) was...

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PMID: 8739779
DOI: 10.2169/internalmedicine.35.266

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Mass screening for complete deficiency of thyroxine-binding globulin in adult Japanese by comprehensive health examination.PMID 8739779Read ↗

Gene screening of 23 Japanese families with complete thyroxine-binding globulin deficiency: identification of a nucleotide deletion at codon 352 as a common cause.Semantic proximity Read ↗

Gene screening of thyroxine-binding globulin (TBG) deficiencies in the Japanese: only two mutations account for TBG deficiencies in the Japanese.Semantic proximity Read ↗

Gene screening in Japanese families with complete deficiency of thyroxine-binding globulin demonstrates that a nucleotide deletion at codon 352 may be a race specific mutation.Semantic proximity Read ↗

Familial thyroxine-binding globulin deficiency associated with hyperthyroidism.Semantic proximity Read ↗

Thyroxine-binding globulin variant (TBG-Kumamoto): identification of a point mutation and genotype analysis of its family.Semantic proximity Read ↗

Molecular analysis of females manifesting thyroxine-binding globulin (TBG) deficiency: selective X-chromosome inactivation responsible for the difference between phenotype and genotype in TBG-deficient females.Semantic proximity Read ↗

A truncated thyroxine-binding globulin due to a frameshift mutation is retained within the rough endoplasmic reticulum: a possible mechanism of complete thyroxine-binding globulin deficiency in Japanese.Semantic proximity Read ↗

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