Three novel mutations causing complete t4-binding globulin deficiency

Journal of Clinical Endocrinology and Metabolism

Volumn 86, Issue 10, 2001, Pages 5039-5044

  Reutrakul, Sirimon ^a   Janssen, Onno E ^b   Refetoff, Samuel ^a  

^a UNIVERSITY OF CHICAGO   (United States)

^b UNIVERSITY OF DUISBURG ESSEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

THYROXINE; THYROXINE BINDING GLOBULIN;

ADULT; ALLELE; AMINO ACID SEQUENCE; ARTICLE; CODON; CONTROLLED STUDY; FEMALE; FRAMESHIFT MUTATION; GENE DELETION; GENE MUTATION; GENE SEQUENCE; HORMONE DEFICIENCY; HUMAN; HUMAN TISSUE; INFANT; MALE; PHENOTYPE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; STRUCTURE ANALYSIS; THYROXINE BINDING GLOBULIN DEFICIENCY; THYROXINE BLOOD LEVEL; TURNER SYNDROME;

EID: 0034750211     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jcem.86.10.7916     Document Type: Article

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