Gene screening of thyroxine-binding globulin (TBG) deficiencies in the Japanese: Only two mutations account for TBG deficiencies in the Japanese

Journal of Clinical Endocrinology and Metabolism

Volumn 81, Issue 2, 1996, Pages 580-585

  Inagaki, Akemi ^a   Miura, Yoshitaka ^a   Mori, Yuichi ^a   Saito, Hidehiko ^a   Seo, Hisao ^b   Oiso, Yutaka ^a  

^a NAGOYA UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b NAGOYA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; LIOTHYRONINE; THYROXINE; THYROXINE BINDING GLOBULIN;

ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; ETHNIC GROUP; FEMALE; GENE MUTATION; GENETIC DISORDER; GENETIC SCREENING; HUMAN; JAPAN; MALE; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; THYROID DISEASE; THYROID FUNCTION TEST; X CHROMOSOME LINKAGE;

ALLELES; BASE SEQUENCE; CODON; FEMALE; GENE DELETION; HETEROZYGOTE; HUMANS; JAPAN; MALE; MOLECULAR SEQUENCE DATA; MUTATION; POLYMERASE CHAIN REACTION; THYROXINE-BINDING PROTEINS;

EID: 0030021725     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jc.81.2.580     Document Type: Article

References (31)

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